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22/07/2008 Chemical Stability of an Admixture Combining Ziconotide and Bupivacaine During Simulated Intrathecal Administration David Shields, Rick Montenegro, Jennifer Aclan Neuromodulation 2007 ; 10 : 1-5.
18/07/2008 Paul M, Lahlou A, Carvalho M, Blanchet B, Astier A. Thermal stability of two monoclonal antibodies : cetuximab and bevacizumab. EJOP 2008 ; 2, 1 : 37.
15/07/2008 Formulation and thermal sterile stability of a less painful intravenous clarithromycin emulsion containing vitamin E Pages 47-56 Yan Lu, YanJiao Wang and Xing Tang Int J Pharm 2008; 546+, 1-2: 47-56.
11/07/2008 Anti-Xa Stability of Diluted Dalteparin for Pediatric Use Neil A Goldenberg, Linda Jacobson, Hannah Hathaway, Mark Tripputi, Judy Primeaux, Jason Child Ann of Pharmacother2008, 42, 4: 511-515
08/07/2008 Stability of cefuroxime in BSS solution. This new poster was presented at the XII Congress of the French Sociiety of Clinical Pharmacists in February 2008 (Saint malo - France) The poster can be downloaded. See in "Publication" and "Stability and compatibility" With the authorization of the authors.
04/07/2008 Identification and quantification of degradations in the Asp–Asp motifs of a recombinant monoclonal antibody Gang Xiao , and Pavel V. Bondarenko Journal of Pharmaceutical and Biomedical Analysis Volume 47, Issue 1, 12 May 2008, Pages 23-30
01/07/2008 Improving the stability of potassium clavulanate in admixture with amoxicillin By Elena M. Vega, BSc, PhD, Ruben H. Manzo, BSc, PhD and Nancy Sola, BSc, PhD Hospital Pharmacist 2008;15:183-185
27/06/2008 Silicate release from glass for pharmaceutical preparations Denise Bohre , Fabiana Bortoluzzi, Paulo Cícero Nascimento, Leandro Machado Carvalhoa and Adrian Gustavo Ramirez International Journal of Pharmaceutics 2008, 355, 1-2 : 174-183.
24/06/2008 Stability of proteins encapsulated in injectable and biodegradable poly(lactide-co-glycolide)-glucose millicylinders Jichao Kang, Oliver Lambert , Michael Ausborn and Steven P. Schwendeman International Journal of Pharmaceutics 2008, 357, 1-2: 235-243.
20/06/2008 Stability of metoprolol tartrate injection 1 mg/mL undiluted and 0.5 mg/mL in 0.9% sodium chloride injection and 5% dextrose injection Michael D. Kraft, Cary E. Johnson, Christopher Chung and Frank Julian American Journal of Health-System Pharmacy, Vol. 65, Issue 7, 636-638 2008
17/06/2008 Stability of Levalbuterol in a Mixture of Levalbuterol and Ipratropium Nebulizer Solution Weeranuj Yamreudeewong, M. Glaucia Teixeira, and Gabriele E. Mayer Hosp Pharm 2008; 43: 303-306.
13/06/2008 Physicochemical Stability of Parenteral Nutrition Supplied as All-in-One for Neonates Maria Skouroliakou, Chrysoula Matthaiou, Antonia Chiou, Demosthenes Panagiotakos, Antonis Gounaris, Tony Nunn and Nikolaos Andrikopoulos. Journal of Parenteral and Enteral Nutrition, Vol. 32, No. 2, 2008 201-209
10/06/2008 Two news poster on the stability of cytotoxic drugs can be downloaded . See in "Publications" and "Stability and compatibility"
06/06/2008 Trusley C, Ben M, Kupiec TC, Trissel LA. Compatibility and stability of palonosetron hydrochloride with four neuromuscular blocking agents during simulated Y-site administration. Int J Pharm Compound 2008; 12, 2: 156-160.
03/06/2008 Kupiec T, Ben M, Trusley C, Trissel LA. Compartibility and stability of palonosetron hydrochloride with gentamicin, metronidazole, or vancomycin during simulated Y-sirte administration. Int J Pharm Compound 2008; 12,2: 170-173.
30/05/2008 Degradation of paclitaxel and related compounds in aqueous solutions I: Epimerization Jiaher Tian , Valentino J. Stella. J Pharm Sci 2008; 97, 3: 1224-1235.
27/05/2008 Continuous versus intermittent infusion of temocillin, a directed spectrum penicillin for intensive care patients with nosocomial pneumonia: stability, compatibility, population pharmacokinetic studies and breakpoint selection Raf De Jongh1, Ria Hens1, Violetta Basma2, Johan W. Mouton3, Paul M. Tulkens2,* and Stéphane Carryn2 J Antimicrob Chemother 2008 ; 61, 2 : 382-388.
23/05/2008 Gupta V.D. Chemical stability of tramadol hydrochloride injection. Int J Pharm Compound 2008; 12, 2: 161-162.
20/05/2008 Stability of TPN: influence of electrolytes You can download the pdf file of this docuent (in english) on the website of the Unicersity Hospital of Lausanne (Switzerland) (after the opening, click on « Stabilité des TPN: influence des électrolytes » http://www.chuv.ch/pha/pha_home/pha_enseignement/pha_ens_seminaires.htm
16/05/2008 Stability of Bortezomib Reconstituted with 0.9% Sodium Chloride at 4°C and Room Temperature (23°C) Scott E Walker, Debbie Milliken, and Shirley Law Can J hosp Pharm 2008; 61, 1
13/05/2008 Chemical stability of haloperidol injection by high performance thin-layer chromatography Sigrid Mennickent, Loreto Pino , Mario Vega , Marta de Diego J Sep Sci 2008 ; 31, 1 : 201-206.
09/05/2008 Risks associated to injectable drugs You can download the pdf file of this docuent (in english) on the website of the Unicersity Hospital of Lausanne (Switzerland) (after the opening, click on « Risques liés aux médicaments injectables » http://www.chuv.ch/pha/pha_home/pha_enseignement/pha_ens_seminaires.htm
06/05/2008 Total parenteral nutrition – problems in compatibility and stability Allan Mikael Schroder EJHP Practice 2008; 14, 1: 65-67.
02/05/2008 Visual compatibility of caspofungin acetate with commonly used drugs during simulated Y-site delivery Chad K. Condie, Linda S. Tyler, Brian Barker and David M. Canann American Journal of Health-System Pharmacy, Vol. 65, Issue 5, 454-457
29/04/2008 Extended stability of iobenguane under simulated clinical conditions George H. Hinkle, Jillian V. Dura, Richard S. Morosco and Milap C. Nahata American Journal of Health-System Pharmacy, Vol. 65, Issue 2, 142-144
25/04/2008 Study of protein conformational stability and integrity using calorimetry and FT-Raman spectroscopy correlated with enzymatic activity A.A. Elkordy , a, , R.T. Forbesa and B.W. Barrya Eur J Pharm Sci 2008; 33, 2: 177-190.
22/04/2008 Calcium and phosphate compatibility: Revisited again David W. Newton and David F. Driscoll Am J Health Syst Pharm 2008 65: 73-80.
18/04/2008 Strategy for identification of leachables in packaged pharmaceutical liquid formulations Changkang Pan, Ferris Harmo, Karen Toscano, Frances Liu and Richard Vivilecchia J Pharm Biomed Anal 2008; 46, 3: 520-527.
15/04/2008 A new poster can be freely downloaded. See "Publications" and "Stability and compatibility" Comparative of different intravenous infusion containers. This poster was presented at the 10th Congress of the European Association of Hospital Pharmacists. Lison, Portugal, 16-18 March 2005.
11/04/2008 Hong Yao Zhanga, Xing Tang , a, , Hong Ying Lia and Xiao Liang Liua A lipid microsphere vehicle for vinorelbine: Stability, safety and pharmacokinetics International Journal of Pharmaceutics 2008;348 ,1-2: 70-79
08/04/2008 Adwoa O. Nornooa, Diana S.-L. Chowb Cremophor-free intravenous microemulsions for paclitaxel II. Stability, in vitro release and pharmacokinetics International Journal of Pharmaceutics 208; 349, Issues 1-2, 117-123
04/04/2008 Victoria F. Samanidou , Evaggelia N. Evaggelopoulou, Ioannis N. Papadoyannis Development of a validated HPLC method for the determination of four penicillin antibiotics in pharmaceuticals and human biological fluids Journal of Separation Science 2006 ; 29, 11 : 1550-1560.
01/04/2008 Tiffany Derrick, Adeola O. Grillo, Samadhi N. Vitharana, LaToya Jones, Jason Rexroad, Ambarish Shah, Melissa Perkins, Thomas M. Spitznagel, C. Russell Middaugh. Effect of polyanions on the structure and stability of repiferminTM (keratinocyte growth factor-2) J Pharm Sci 2007; 96, 4: 761-776.
28/03/2008 Frederic Adnet, Laurence Le Moyec, Charles E Smith, Michel Galinski, Patricia Jabre1, Frederic Lapostolle Stability of succinylcholine solutions stored at room temperature studied by nuclear magnetic resonance spectroscopy Emergency Medicine Journal 2007;24:168-169
25/03/2008 Kupiec Thomas C, Skinner Rodney, Lanier Lance Quality-Control Analytical Methods: Stability Versus Potency Testing: The Madness is in the Method Int J Pharm Compound 2008 ; 12, 1 : 50-53
21/03/2008 Stability of Injectable Oxytocics in Tropical Climates: Results of Field Surveys and Simulation Studies on Ergometrine, Methylergometrine and Oxytocin - EDM Research Series N° 08 On WHO website
18/03/2008 Roberto Sacco, Giovanna Sacchetto, Mirella Francalanci, Cinzia Boselli Studio di stabilità chimico-fisica di una formulazione per la terapia antalgica a base di levobupivacaina e fentanyl Bolletino SIFO 2-2006
11/03/2008
Roy Julie J, Boismenu Daniel, Mamer Orval A, Nguyen Bao T, Forest Jean-Marc, Hildgen Patrice Room Temperature Stability of Injectable Succinylcholine Dichloride Int J Pharm Compound 2008 ; 12, 1 : 83-85.
07/03/2008 Cristiana Romanazzi, Stella Sferra, Anna Campi, Barbara Rabino, Marco Barbieri, Sofia Castellani, Luana Sabbatini, Paola Scanavacca Dexrazoxane: stabilità in soluzione Bolletino SIFO 2007;53 ,4 : 178-180
04/03/2008 Development of a validated HPLC method for the determination of four penicillin antibiotics in pharmaceuticals and human biological fluids Victoria F. Samanidou , Evaggelia N. Evaggelopoulou, Ioannis N. Papadoyannis Journal of Separation Science 2006 ; 29, 11 : 1550-1560.
29/02/2008 Stabilis online ! Click on "Stabilis" on the left side on the screen and then click on the button "Stabilis" By choosing "List of drugs", you have access to 374 monographs of injectable drugs with informations on stability in solutions, in admixtures, incompatibilities ...
29/02/2008 Stability of a mixture of technetium Tc 99m sulfur colloid and lidocaine hydrochloride Jillian V. Dura and George H. Hinkle Am J Health Syst Pharm 2007; 64, 23: 2477-2479.
26/02/2008 A Comparison of Plasticizers for Use in Flexible Vinyl Medical Products Data from three studies suggest that using trimellitates can reduce the amount of plasticizer that may migrate from PVC devices. Richard C. Adams Medical Device Link dec 2007
22/02/2008 Diethylhexylphthalate Extracted by Typical Newborn Lipid Emulsions From Polyvinylchloride Infusion Systems Causes Significant Changes in Histology of Rabbit Liver P. D. Steffan Loff, Ulrike Subotic, Jasmina Oulmi-Kagermann, Bettina Kränzlin, Maria-Franziska Reinecke and Christiane Staude Journal of Parenteral and Enteral Nutrition, Vol. 31, No. 3, 2007 188-193
19/02/2008 New links to articles or posters have been placed into the list "Stability and compatibility". See "Publications" and "Stability and compatibility".
12/02/2008 Chemical stability of midazolam injection by high performance liquid chromatography Marta de Diego, Gloria Godoy,Sigrid Mennickent Journal of Separation Science 2007 ; 30, 12 : 1833-1838.
11/02/2008 STABILIS online ! The database STABILIS is now available on the website. You have to choose "Stabilis" on the menu at the left side of the screen. The database contains important improvements like a general search function, a search function for incompatibilities, possibility to create a pdf file for each monograph etc. Don't hesitate to give your opinion about the new Stabilis database by using the email adress : infostab@wanadoo.fr
29/01/2008 An alternative to DEHP plasticized polyvinyl chloride in chemotherapy drug delivery systems Len Czuba, Harry Puryear, Kamal Sarkar. Journal of Vinyl and Additive Technology 2004 ; 2, 4 : 314-320.
25/01/2008 Dual effects on Tween 80 on protein stability Wang W, Wang Y.J, D.Q. Wang D.Q. Int J Pharm 2008 ; 347, 1-2 : 31-38.
22/01/2008 Palonosetron Hydrochloride Compatibility and Stability with Three Beta-Lactam Antibiotics During Simulated Y-Site Administration Ben Michel, Trusley Craig, Kupiec Thomas C, Trissel Lawrence A Int J Pharm Compound 2007; 11, 6: 520-524.
18/01/2008 Tracking of the Kinetic Stability of 2 Types of Total Nutrient Admixtures Containing Different Lipid Emulsions Judit Balogh, Dorottya Kiss, Judit Dredán, István Puskás, Ferenc Csempesz, and Romána Zelkó AAPS PharmSci. 2006; 7(4)
15/01/2008 A rapid technique to evaluate the oxidative stability of a model drug. Felton LA, Yang J, Shah K, Omidian H, Rocca JG Drug Dev Ind Pharm 2007 Jun; 33(6):683-9.
15/01/2008 Stability of 70% alcohol solutions in polypropylene syringes for use in ethanol-lock therapy Mary Petrea Cober and Cary E. Johnson Am J Health Syst Pharm 2007; 64, 23: 2480-2482.
11/01/2008 Evaluation of the chemical compatibility of plastic contact materials and pharmaceutical products; safety considerations related to extractables and leachables Dennis Jenke * J Pharm Sci 2007; 96, 10: 2566-2581.
08/01/2008 Stability of vecuronium in sterile water for injection stored in polypropylene syringes for 21 days Cary E. Johnson and Mary Petrea Cober Am J Health Syst Pharm 2007; 64, 22: 2356-2358.
04/01/2008 de Diego M, Godoy G, Mennickent S Chemical stability of midazolam injection by high performance liquid chromatography. J Sep Sci 2007 Jun 12.
01/01/2008 Compatibility and stability of tramadol and dexamethasone in solution and its use in terminally ill patients S. Negro, A. Salam, Y. Sánchez, M. L. Azuara, E. Barcia. J Clin Pharm Ther 2007; 32, 5: 441-444.
28/12/2007 Amélioration des pratiques d’administration des antibiotiques injectables : proposition et évaluation d’un guide de compatibilité physico-chimique (in french) A Camut, V Noirez, B Gustin, A Khalife J Pharm Clin 2007; 26, 3: 143-150.
25/12/2007 Accelerated aging: Prediction of chemical stability of pharmaceuticals Kenneth C. Waterman , and Roger C. Adami Int J Pharm 2005; 293, 1-2: 101-125.
21/12/2007 A Four-Column Approach to Developing Stability-Indicating HPLC Methods This article describes a method development approach that uses different packing materials and mobile-phase pH levels to optimize the chromatographic separation of degradation products from active ingredients. LCGC North America, Jun 1, 2002
18/12/2007 Liposomal amphotericin B eye drops to treat fungal keratitis: Physico-chemical and formulation stability K. Morand, A.C. Bartoletti, A. Bochot, G. Barratt, M.L. Brandely and F. Chast Int J Pharm 2007; 334, 1-2: 150-153.
14/12/2007 Influence du stress mécamique sur la stabilité du bévacizumab. (in french) Lahlou, Blanchet B, Carvalho M, Astier A, Paul M. Presented at the SFPO Congress in Nice (october 2007) Can be downloaded. See "Publications" and "Stability and compatibility" With the authorization of the author.
11/12/2007 Liposome formulation of Paclitaxel with enhanced solubility and stability. Yang T, Cui FD, Choi MK, Lin H, Chung SJ, Shim CK, Kim DD Drug Deliv 2007 Jun; 14(5):301-8.
07/12/2007 Stability and degradation kinetics of etoposide-loaded parenteral lipid emulsion. Tian L, He H, Tang X J Pharm Sci 2007 May 14.
04/12/2007 Stabilité thermique de 2 anticorps monoclonaux : bevacizumab et cetuximab. (in french) Paul M, Lahlou A, Carvahlo M, Blanchet B, Astier A. Presented at the SFPO Congress in Nice (october 2007) Can be downloaded. See "Publications" and "Stability and compatibility" With the authorization of the author.
30/11/2007 Stability of Docetaxel Solution after Dilution in Ethanol and Storage in Vials and after Dilution in Normal Saline and Storage in Bags. Scott E Walker, Flay Charbonneau, and Shirley Law Can J Hosp Pharm 2007; 60, 5: 217-284.
27/11/2007 Are monoclonal antibody stable ? (in french) Pr Alain ASTIER Presented at the SFPO Congress in Nice (october 2007) Can be downloaded. See "Publications" and "Stability and compatibility" With the authorization of the author.
23/11/2007 A sequential temperature cycling study for the investigation of carboplatin infusion stability to facilitate 'dose-banding'. Kaestner S, Sewell G. In this study, the authors have demonstrated that carboplatine infusions could be stored refrigerated for 84 days. J Oncol Pharm Practice 2007; 13: 119-126.
20/11/2007 Examination of stability and compatibility of flucloxacillin (Floxapen®) and ceftazidime (Fortum®) in two infusion media: relevance for the clinical praxis. Florian Thalhammer, Alexandra Maier-Salamon und Walter Jäger. Wien Med Wochenschr 2005 ; 155 (13-14) : 337-343.
16/11/2007 Compatibility of insulin over 24 hours in standard and bicarbonate-based peritoneal dialysis solutions contained in bags made of different materials. Voges M, Divino-Filho JC, Faict D, Somers F, Vermeulen P. Perit Dial Int 2006 Jul-Aug; 26(4) :498-502.
13/11/2007 Pathological Consequences From the Infusion of Unstable Lipid Emulsion Admixtures in Guinea Pigs. Todd Canada. Nutrition in Clinical Practice 2006; 21, 6: 636-637.
09/11/2007 Stability and compatibility of histamine H2-receptor antagonists in parenteral nutrition mixtures. Puzovic M, Hardy G. Curr Opin Clin Nutr Metab Care 2007 May; 10(3) :311-7.
09/11/2007 Physicochemical stability of lipid injectable emulsions: Correlating changes in large globule distributions with phase separation behavior. Thomas Gonyon, Pankaj Patel, Heather Owen, Andrew J. Dunham and Phillip W. Carter. Int J Pharm 2007; 343, 1-2: 208-219.
06/11/2007 Estabilidad de parecoxib en dilución con otros fármacos y administrado en perfusión continua IV para el control del dolor postoperatorio. Acín Lázaro MP, Bono Ariño C, Martínez Bazán R, Manzanares Marín I, Faci Bouthelier A, Velamazán Blocona MJ, Facorro Gaspar E, Sanz Gandasegui M, Aleploglian Barbarian K Investig. Clin. Farm. 2005, Vol. 2 (4): 195-203
02/11/2007 Stability of oxaliplatin in infusion bags containing 5% dextrose injection. Pascal André, Salvatore Cisternino, Anne-Lise Roy, Fouad Chiadmi, Joël Schlatter, Pascal Agranat, Olivier Fain and Jean-Eudes Fontan Conclusion. Oxaliplatin 0.7 mg/mL in infusion bags containing 5% dextrose injection was chemically stable for at least 30 days at both 3–7 °C and 20–24 °C without regard to light exposure. Am J Health-Syst Pharm,2007;64,18/1950-1954
30/10/2007 Use of microcalorimetry and its correlation with size exclusion chromatography for rapid screening of the physical stability of large pharmaceutical proteins in solution. Burton L, Gandhi R, Duke G, Paborji M Pharm Dev Technol 2007; 12(3) :265-73.
26/10/2007 Validation of an HPLC method for the analysis of decomposition products in injectable diazepam. Hudecová T, Bátorová V, Hatrík S, Havránek E Ceska Slov Farm 2004 Sep; 53(5) :228-33.
23/10/2007 Compatibility and stability of furosemide and dexamethasone combined in infusion solutions. Negro S, Rendon AL, Azuara ML, Sánchez Y, Fernández-Carballido A, Barcia E These results confirm the stability of mixtures prepared with sodium furosemide (< or = 120 mg/day) and dexamethasone sodium phosphate (< or = 40 mg/day) for a period of 5 days and with independence of their storage at 4 degrees C or 25 degrees C. Arzneimittelforschung 2006; 56(10) :714-20.
19/10/2007 Long-term stability of sodium folinate in dextrose 5% polyolefin bags at 4°C. Cadrobbi J, Hecq JD, Vanbeckbergen D, Jamart J, Galanti L. J Oncol Pharm Practice 2007; 13: 99-103.
16/10/2007 Shelf-lives of IV products — are there any limits? By Michael Allwood, PhD, FRPharmS and Graham Sewell, PhD, MRPharmS Hospital Pharmacist 2007;14:242
12/10/2007 Ortega Valín L, del Pozo Ruiz JJ. Cómo y por qué estudiar la estabilidad de las mezclas de fármacos para uso intravenoso Investig. Clin. Farm. 2006, Vol. 3 (3): 130-135
09/10/2007 Mário L de Lemos, Linda Hamata Stability issues of parenteral chemotherapy drugs Journal of Oncology Pharmacy Practice, Vol. 13, No. 1, 27-31 (2007)
05/10/2007 A simulation study with statistical evaluation for the determination of non-isothermal kinetics conditions in drugs stability Eur J Pharm Sci; 2007; 31, 5: 277-287.
02/10/2007 Stability of an extemporaneously prepared recombinant human interferon alfa-2b eye drop formulation. Conclusion. An extemporaneously pre -pared rh-IFN- 2b eye drop formulation was stable at 5 ± 3 °C for 15 days and at 28 ± 2 °C for 7 days. Am J Health Syst Pharm; 64, 16: 1716-1719.
28/09/2007 Incompatibility reactions in iv drug therapy : Preventable medication errors. Presented by Pr Stefan Muhlebach, Bern, Switzerland during the EAHP congress in Bordeaux, France, march 2007. You can download the pdf file. See in "Publications" and "Stability and compatibility" With the authorization of the author.
25/09/2007 Incompatibility of iv drugs in daily practice : an underrecognised and underestimated problem. by Karin Nemec, PhD from Vienna, Austria Presented during the seminar "Incompatibility reactions in drug therapy – preventable medication errors" in the EAHP Congress in Bordeaux, France, march 2007. You can download the pdf file. See in "Publications" and "Stability and compatibility" With the authorization of the author
21/09/2007 Room-temperature storage of medications labeled for refrigeration. Conclusion. Information regarding the room-temperature storage of 79 medications labeled for refrigerated storage was compiled. Am J Health Syst Pharm 2007; 64, 16: 1711-1715.
18/09/2007 Viability of micro-organisms in novel anticancer drug solutions. Conclusion : Micro-organisms can survive in diluted solutions of antineoplastic drugs and proliferate when transferred to proper growth media. EJHP-Science 2007; 13, 2: 27-32.
14/09/2007 Development and validation of a simple HPLC method for simultaneous in vitro determination of amoxicillin and metronidazole at single wavelength. J Pharm Biomed Anal 2007; 43, 1: 325-329.
11/09/2007 Stability issues of parenteral chemotherapy drugs. J oncol Pharm Practice 2007; 13: 27-31.
07/09/2007 Stability of a heparin-free 50% ethanol lock solution for central venous catheters. These findings suggest that a 50% (v/v) ethanol solution stored in a syringe at room temperature, not protected from light is stable over a 28 day period J Oncol Pharm Practice 2007; 13: 33-37.
03/09/2007 Hitchingham L, Thomas VH. Development of a semi-automated chemical stability system to analyse solution based formulations in support of discovery candidate selection. This paper describes the semi-automated chemical stability system (SACSS) set-up, method validation and use. This process has proven to be a good indicator of chemical and physical stability in greater than 90% of the compounds tested. Ref : J Pharm Biomed Anal 2007; 43: 522-526.
03/09/2007 Development and validation of a stability-indicating analytical method for the quantitation of oxytocin in pharmaceutical dosage forms J Pharm Biomed Anal 2007;43,1: 179-185.
31/08/2007 Stability and degradation kinetics of etoposide-loaded parenteral lipid emulsion The shelf life (T90%) of etoposide in lipid emulsion was estimated to be 47 days at 25°C and it would be stable when stored for 427 days at 4°C, which is a significant improvement compared with a stability of 9.5 days in aqueous solution at 25°C. J Pharm Sci 2007; 96, 7: 1719-1726.
28/08/2007 Stability of palonosetron in Y-site Physical and chemical stability of palonosetron with metoclopramide and promethazine during simulated Y-site administration. Results : Palonosetron hydrochloride is physically compatible and chemically stable with undiluted metoclopramide hydrochloride and also with promethazine hydrochloride diluted in 5% dextrose injection during simulated Y-site administration. Ref: Int J Pharm Compound 2007 ; 11, 1 : 82-85
24/08/2007 Physical compatibility and chemical stability of mycophenolate mofetil during simulated Y-site administration with commonly coadministered drugs Conclusion. Mycophenolate mofetil was physically compatible and chemically stable with vancomycin, cefepime, norepinephrine, dopamine, and tacrolimus for up to four hours of simulated Y-site administration. The physical compatibility of mycophenolate mofetil with cyclosporine could not be confirmed. Am J Health Syst Pharm 2007; 64, 13, 1410-1414.
21/08/2007 Tramadol and hyoscine N-butyl bromide combined in infusion solutions: compatibility and stability. In this study, the authors have demonstrated that Tramadol HCl (100-400 mg/day) can be formulated together in saline with hyoscin N-butyl bromide (dose range 40-80 mg/day) for sc infusion using a 60 ml drug infuser for a duration of 7 days. Ref : Support Care Cancer 2007; 15: 57-62.
17/08/2007 Quantitative analysis of in vitro compatibility of binary and ternary mixtures of nitroimidazole and macrolides in combination with omeprazole using a calorimetric technique Conclusion: The results suggest compatibility of drug pairs in their binary mixtures. However, ternary mixtures show somewhat larger interactions. The magnitude of interaction enthalpy of a ternary mixture comprising tinidazole, clarithromycin and omeprazoles which are available as a marketed kits has been calculated to be significant, suggesting that the three drugs cannot be co-formulated. Pharmazie 2007; 62, 5: 327-336.
14/08/2007 Xiao B, Gozo SK, Herz L. Development and validation of HPLC methods for the determination of potential extractables from elastomeric stoppers in the presence of a complex surfactant vehicle used in the preparation of parenteral drug products. J Pharm Biomed Anal 2007; 43: 558-565. In this paper, HPLC methods were developped and validated for potential extractables from commercial elastomeric stoppers in a complex surfactant matrix.
07/08/2007 Peut-on conditionner les solutions de docétaxel dans des poches en PVC ? In this paper, the authors have demonstrated that docetaxel solutions were stable for 48 hours in PVC and poyethylene containers. However, PVC infusion bags should be avoided because the leaching of plasticizer after the injection of docetaxel. The DEHP concentration increases with time. J Pharm Clin 2006; 25, 3: 147-152.
03/08/2007 Quantitative analysis of in vitro compatibility of binary and ternary mixtures of nitroimidazole and macrolides in combination with omeprazole using a calorimetric technique Conclusion: The results suggest compatibility of drug pairs in their binary mixtures. However, ternary mixtures show somewhat larger interactions. The magnitude of interaction enthalpy of a ternary mixture comprising tinidazole, clarithromycin and omeprazoles which are available as a marketed kits has been calculated to be significant, suggesting that the three drugs cannot be co-formulated. Pharmazie 2007; 62, 5: 327-336.
31/07/2007 Physical stability of 20% lipid injectable emulsions via simulated syringe infusion: Effects of glass vs plastic product packaging. J Parent and Enter Nutr 2007; 31, 2: 148-153.
27/07/2007 Stability of busulfan in polypropylene syringes Busulfan injection (Busilvex®, Busulfex) stored in B/Braun syringes at 18-20°C without light protection or refrigerated was stable for up to 28 days. Unused busulfan injection is not necessarily to be discarded but can be stored for a prolonged period of time in a rubber free syringe, preferably under refrigeration. Ref: Pharmazie 2006; 61: 845-850.
24/07/2007 Stability of ertapenem in aqueous solutions. In
this study the kinetics of ertapenem was studied in aqueous solutions
at various pH by using two HPLC methods. Ertapenem has the greatest
stability at pH 5-6. Ref : J Pharm Biomed Anal 2007; 43: 445-449.
20/07/2007 Stability of oxytocin Oxytocin was demonstrated to be physically and chemically stable when admixed in 5% dextrose injection or 0.9% sodium chloride inujection for 90 days and stored at room temperature (near 23°C). However, oxytocin in lactated Ringer’s injection should be restricted to a use period no longer than 28 days at room temperature to prevent microprecipitate formation and drug loss. Ref: Int J Pharm Compound 2006; 10, 2: 156-158.
17/07/2007 A physical and chemical stability of amphotericin B lipid complexes (Abelcet)after dilution in dextrose 5%. EJHP-Science 2007; 13, 1: 10-13.
13/07/2007 Isolation and characterisation of degradation impurities in docetaxel drug substances and its formulation. J pharm Biomed Anal 2007; 43: 1228-1235.
10/07/2007 Stability of pemetrexed 25 mg/ml in a glass vial and 5 mg/ml stored in a PVC container after storage for one month at 2-8°C. EJHP-Science 2007; 13, 1: 14-16.
06/07/2007 Recent developments on long-term stability test conditions. Singh S, Kumar V. This article can be downloaded on the website of the American Association of Pharmaceutical Scientis http://www.aapspharmaceutica.com/inside/focus_groups/Stability/index.asp#top
03/07/2007 Incompatibility of phenytoin Incompatibility: Phenytoin is incompatible with vasopressin by immediate formation of a precipitate. Ref: Am J Health Syst Pharm 2005; 62: 1969-1976.
29/06/2007 Drug compatibility with new polyolefin infusion solution containers Of the seven drugs subject to sorption to PVC, only insulin showed a substantial loss in the VISIV containers. Carmustine exhibited a loss consistent with the drug’s known chemical stability. None of the drugs that are known to leach plastic components, such as DEHP plasticizer, from PVC equipment exhibited any leached components in the VISIV containers. Ref: Am J Health Syst Pharm 2006; 63: 2379-2382.
26/06/2007 «Stability studies – Assessment experience » was presented at the WHO training workshop on pharmaceutical quality, GMP and bioequivalence with a focus on artemisenines. Guilin, China, 9 January 2006 by Pr JANOS POGANY. http://mednet3.who.int/prequal/trainingresources/pq_pres/workshop_China_Jan2006/StabilityStudies.ppt
22/06/2007 Stability of moxifloxacin injection in peritoneal dialysis solution bags (Dianeal PD1 1·36%® and Dianeal PD1 3·86%®) The mean moxifloxacin concentration in the Dianeal PD1 1·36% solution remained ≥90% of the initial concentration for 14 days at 4 °C, 7 days at 25 °C and 3 days at 37 °C. For Dianeal PD1 3·86%® moxifloxacin concentrations remained ≥90% for 14 days at 4 °C, 3 days at 25 °C and 12 h at 37 °C. Ref: J Clin Pharm Ther 2006; 31: 641-643.
19/06/2007 Stability studies of drugs used in oncology : the role of the hospital pharmacist Published in EJHP practice 2006, 6 : 75-76.
15/06/2007 Stability of vancomycine Vancomycine hydrochloride in 5% dextrose polyolefin bags may be frozen and thawed in a microwave oven without major changes that affect concentration. Subsequent storage of the bags at 4°C is possible for at least 56 days. Within those limits, vancomycin can be prepared in advance by a centralized service, frozen, thawed and stored under refrigeration for a few days before use in hospital wards Ref: EJHP-S 2005; 11, 5: 111-113.
12/06/2007 Physical and chemical stability of palonosetron hydrochloride with five opiate agonists during simulated Y-site administration Conclusion. Palonosetron hydrochloride was physically and chemically stable with fentanyl citrate, hydromorphone hydrochloride, meperidine hydrochloride, morphine sulfate, and sufentanil citrate during simulated Y-site administration. Am J Health Syst Pharm 2007; 64,11: 1209-1213.
08/06/2007 Stability of mitomycine C for intraperitoneal administration Poster présented at Synprefh Congress in France may 2006 Can be downloaded : see in "Publications" >> "Stability and compatibility"
05/06/2007 Stability of phenylephrine hydrochloride injection in polypropylene syringes Conclusion. Phenylephrine hydrochloride diluted to a concentration of 100 µg/mL in 0.9% sodium chloride injection was stable for at least 30 days when stored in polypropylene syringes at –20 °C, 3–5 °C, and 23–25 °C. Am J Health Syst Pharm 2007; 64, 10: 1092-1095.
01/06/2007 Stabilis 3 a european database on the stability and compatibiity of injectable drugs. In EJHP 2006, 6: 77-78.
29/05/2007 Ketamine incompatibility Physical incompatibilities were observed between ketamine and acyclovir, ampicilline, sodium bicarbonate, furosemide, heparin, insulin, meropenem, phenytoin, potassium phosphate, trimethoprim/sulfametoxazole. Ref: Pharmactuel 2006; 39, 2: 71-75.
25/05/2007 Stability of dolasetron Dolasetron mesylate solutions (Anzemet®)) 20 mg/ml in syringes are stable for up to eight months at room temperature Ref: Am J Health Syst Pharm 2005; 62: 896-899.
22/05/2007 Long-term physical and chemical stability of a generic paclitaxel infusion The stability of paclitaxel was limited by physical stability and this was dependent on paclitaxel concentration in the infusion, diluent used and the storage temperature. Ref: EJHP-S 2006; 12, 6: 129-134.
19/05/2007 Send your posters to the INFOSTAB website ! You have recently presented a poster on stability or compatibility of injectable drugs during a congress. You can now present your research to the hospital pharmaceutical community by publishing your poster in the Infostab website (in "Publications" and "Stability and compatibility"). Send your poster in pdf format to the following address: infostab@wanadoo.fr
18/05/2007 Stability of ondansetron + methylprednisolone + clorazepate dipotassium diluted in dextrose 5% : you can download the poster which has be presented at the Hopipharm Congress in France in mai 2006. (poster in french).
See in the menu : "Publications" and "Stabilité and compatibilité"
15/05/2007 Stability of vancomycin in syringes The vancomycin (5 mg/ml) was found to be chemically and microbiologically stable at 4°C for 6 months. Losses were important after 14 days at 25°C.The samples subjected to simulated ward conditions were stable for 48 hours at 25°C. Ref EJHP-S 2006; 12, 6: 135-139.
12/05/2007 Dose banding - Cytotoxic drug standardization : establish the positive list of anticancer drugs to be standardized taking into account pharmacokinetic and stability studies. Workshop at the Gerpac Congress in Belgium (Sunparks Kempense Meren - Mol) October 3-5 2007. First announcement and registration form can be downloaded on the Gerpac webste : http://www.gerpac.org
11/05/2007 Stability of voriconazole Voriconazole injection 2mg/ml, when protected from light, was stable for eight days when stored at 4 or 25°C in 0.9% sodium chloride injection, six days at 4°C in 5% dextrose injection, and four days at 25°C in 5% dextrose injection. Ref: Am J Health Syst pharm 2006; 63: 1426-1426.
08/05/2007 A new interesting link has been created towards the " Association of Pharmaceutical Scientists – Stability focus group" See in "Links" and "Others links"
04/05/2007 World Health Organization (WHO) Stability testing of active substances and pharmaceutical products. This draft guideline can be downloaded on the website of the American Association of Pharmaceutical Scientists (Stability focus group). http://www.aapspharmaceutica.com/inside/focus_groups/Stability/index.asp#top
01/05/2007 The poster "Assessment of injectable drug
administration in two intensive care units and determination of
potential physico-chemical incompatibilities" presented during the EAHP Congress in Geneva (march 2006) can be freely downloaded. See in "Publications" and "Stability and compatibility".
27/04/2007 A new link has been added to present : "Stability-Indicating HPLC Methods for Drug Analysis" from L.A TRISSEL. See in "Link" and "Guidelines"
24/04/2007 "Asean Guideline on stability study of drug products" has been added in the "Guidelines list". See in "Links" and "Guidelines"
20/04/2007 Stability of vancomycin in icodextrin peritoneal dialysis solution. Premixed vancomycin-icodextrin PD solution, whether stored refrigerated or at room temperature, were found to be stable for up to 7 days. Solutions stored at body temperature were stable for up to 24 hours, permitting the practice of prewarming solutions prior to administration. Ref: Ann Pharmacother 2006; 40, 11: 1950-1954.
17/04/2007 Effect of tubing on loss of clonazépam administered by continuous subcutaneous infusion. Significant loss of clonazépam (up to 50%) was observed in all solutions infused through PVC tubing. Solutions infused through non-PVC tubing retained greater than 90% of the initial concentration of clonazepam. It is recommended that when administering clonazepam using a syringe driver, non-PVC tubing be used. Ref: J Pain Sympt Manage 2006; 31, 6: 563-567.
13/04/2007 Stability of ketamine and remifentanil : you can download the poster that has be presented at the EAHP Congress in Geneva in 2006. See in the menu : "Publications" and "Stability and compatibility"
10/04/2007 Stability and compatibility of a meperidine-clonidine mixture. A mixture of meperidine hydrochloride and clonidine remains stable in a PVC-containing reservoir, at room temperature and unprotected from daylight for at least 21 days. Ref: J Pain Symptom Manag 2006; 32, 4: 297-299.
06/04/2007
Study of the compatibility of cefotaxime with tinidazole in glucose injection. In this study, the admixture cefotaxime and tinidazole was stable for 8 hours in dextrose 5%.
J Pharm Biomed Anal 2007; 43: 1849-1853.
05/04/2007 The Infostab website is now translated into 21 languages (italian has been added, translation performed by Camillo Cettuzzi)
03/04/2007 Incompatibility irinotécan/epirubicin A chemical interaction was observed using a spectrophotometric method in the spectra of irinotecan and epirubicin. The chemical interaction occured immediately after admixing and no visual or spectral changes was noticed for 24 hours after the intercation had occured. No sign of physical incompatibility was observed upon visual examination by means of effervescence, pH change, precipitation and colour change. Ref: Cancer Chemother Pharmacol 2005; 56: 529-534.
30/03/2007 Stability of paracetamol-phloroglucinol admixture. Paracetamol and phloroglucinol, prepared by adding phloroglucinol to a glass bottle of paracetamol ready to-use solution, were stable and compatible for up to 48 hours at room temperature without any protection against light. Ref: EJHP-S 2006; 12, 5: 91-95.
30/03/2007 Stability of total nutrient admixtures with lipid injectable emulsions in glass versus plastic packaging. In this paper, the physical stability of two emulsions compounded as part of a total nutrient admixture (TNA) was studied in lipids packaged in either glass or plastic containers. Am j Health Syst Pharm 2007; 64, 4: 396-403. Retour � la liste
28/03/2007 The Infostab website is now translated into 20
languages (turkish has been added, translation
performed by Aygin Bayraktar)
27/03/2007 Stability of palonosetron Palonosetron HCl (Aloxi®) is physically and chemically stable with doxorubicin HCl and epirubicin HCl during simulated Y-site administration of these drugs over 4 hours at ambient room temperature. Ref: Ann Pharmacother 2005; 39: 280-283.
23/03/2007 Stability of tazocilline Tazocin® (piperacillin/tazobactam) was found to be stable in 0.9% sodium chloride in PVC bags for up to 5 days at 7°C and 4 days at room temperature in the light. In non-PVC bags, it was stable for 17 and 3 days respectively. Ref: J Pharm Biomed Anal 2005; 39: 339-343.
20/03/2007 Stability of tramadol and haloperidol The mixture tramadol and haloperidol lactate diluted in NaCl 0.9% in polypropylene syringes is stable for 15 days at room temperature protected from light and in the refrigarator. Ref: J Pain Symptom Manag 2005; 30: 193-199.
16/03/2007 The stability of anticancer drugs by Alain ASTIER EJHP-P 2007, 2: 90-92.
13/03/2007 Stability of dexrazoxane : you can download the poster that will be presented at the EAHP Congress in Bordeaux (France) 21,22,23 march. See in the menu : "Publications" and "Stabilité and compatibilité"
09/03/2007 Stability of palonosetron admixtures Palonosetron hydrochloride was physically and chemically compatible with cyclophosphamide and with ifosfamide during simulated Y-site administration. Ref: Am J Health Syst Pharm 2005; 62: 1998-2000.
02/03/2007 Stability of ondansétron and methylprednisolone Ondansetron 0.16 mg/ml and methylprednisolone 2.4 mg/ml mixed in 50 ml multilayer polyolefin bags (Macoflex N®) were stable in both 5% dextrose injection and 0.9% sodium chloride injection for up to 24 hours at 20-25°C and up to 48 hours at 4-8°C. Ref: Am J Health Syst Pharm 2005; 62, 1: 2001-2005.
02/03/2007 The Infostab website is now translated into 19 languages (slovenian and croatian have been added, translation performed by Silva Pecar Cad and Karin Kasesnik (SLO) and Danijela jonjic (HR))
27/02/2007 Stability of ketorolac tromethamine Ketorolac tromethamine in dextrose 5% 100 ml polyolefin infusion bags may be frozen for 3 months and microwave thawed, without major changes that affect concentration. Ketorolac tromethamine solution may subsequently be stored at 4°C for up to 60 days. Ann Pharmacother 2005; 39: 1654-1658.
23/02/2007 The Infostab website is now translated into 17 languages (russian has beenadded, translation performed by Violeta Kontrimaviciute)
20/02/2007 Stability of dexamethasone and ketamine The mixtures of dexamethasone sodium phosphate (1 mg/14 ml) with ketamine hydrochloride (50 mg/14ml) in 0.9% sodium chloride were physically and chemically stable when stored in plastic syringes at 4°C, 23°C and 37°C and exposed to normal fluorescent light for 8 days. Ref: J Pain Symptom Manage 2005; 30: 80-86.
16/02/2007 The Infostab website is now translated into 16 languages (lithuanian has been added, translation performed by Violeta Kontrimaviciute)
13/02/2007 Palonosetron stability Palonosetron hydrochloride 25µg/ml (Aloxi®) is physically and chemically stable with lorazepam 0.25 mg/ml and midazolam HCl 1 mg/ml in dextrose 5% during simulated Y-site injection. Ref: Int J Pharm Compound 2005; 9, 3: 235-237.
09/02/2007 The Infostab website is now translated into 15 languages (hungarian has been , translation performed by Lívia Sáfrán)
06/02/2007 Stabilnost vorikonazola The solution of voriconazole 4 mg/ml diluted in dextrose 5% in PVC bags is stable for at least 15 days at 4°C. Ref: EJHP-S 2006; 12, 3: 57-59.
02/02/2007 Stability of frozen ceftriaxone Ceftriaxone in 5% dextrose 100 ml polyolefin infusion bags may be frozen and microwave thawed by two different procedures at 270 Watts and 800 Watts power without major changes affecting concentration. Storage at 2°C to 8°C of solution did not affect the stability of the solution for at least 44 days for the 270 Watts cycle and 56 days for the 800 Watts cycle. Ref: EJHP-S 2006; 13, 3: 52-56.
30/01/2007 A new link has been added in the databases towards "Syringe driver"
26/01/2007 Stability of morphine/hyoscine admixture used in palliative care. The admixture morphine hydrochloride (1.37 mg/ml >> 10 mg/ml) with hyscine-Nbutyl bromide diluted with 0.9% sodium chloride is stable for 15 days in polypropylene syringes at room temperature or at 4°C and protected from light. Ref: Support Care Cancer 2005; 13, 4: 239-245.
23/01/2007 Stability of prostaglandin E1 in aqueous solutions. The stability of prostaglandin E1 in physiological serum (NaCl) was assessed considering different factors. Results showed that PGE1 was stable during three months, pH=7, whenstored at 4°C. Ref: EJHP-S 2005; 11, 2: 31-36.
19/01/2007 Stability of doxorubicine and vincristine (VAD regimen) The mixture doxorubicine 1.4 mg/ml with vincristine 0.053 mg/ml is stable in 0.9 sodium chloride or 0.45 sodium chloride/2.5% dextrose for at least 7 days when stored at 8°C. A new, sensitive LC-MS technique in combinaison with UV/fluorescence confirmed these results. Ref: EJHP-S 2006; 1: 10-12.
16/01/2007 Compatibility irinotecan/ leucovorin Rapid degradation of irinotecan was observed in one mixture: irinotecan 0,30mg/ml and leucovorin 3.6 mg/ml. The concentrations of irinotecan were 91.5% after 30 minutes and 76.3% after 24 hours. It was concluded that irinotecan and leucovorin were physically compatible and chemically stable only for a sufficient period of time to allow concurrent infusion via a Y-site. Ref: Can J Hosp Pharm 2005; 58, 4: 212-222.
09/01/2007 Incompatibility of mycafungin Micafungin injection 1.5 mg/ml in 0.9% sodium chloride injection is physically incompatible for 4 hours after simulated Y-site co-administration at room temperature with albumin human, amiodarone, cisatracurium, diltiazem, dobutamine, epinephrine, insulin human regular, labetalol, meperidine, midazolam, morphine sulphate, mycophenolate mofetil, nesiritide, nicardipine, octreotide, ondansetron, phenytoin sodium, rocuronium bromide, vecuronium bromide. Ref : Int J Pharm compound 2006; 10, 3: 230-232.
05/01/2007 Stability of palonosetron/dacarbazine admixture Palonosetron HCl is physically and chemically stable when mixed with dacarbazine during simulated Y-site administration. However palonosetron HCl and methyl prednisolone sodium sucinate are physically incompatible, their admixture resulting in precipitation of methylprednisolone. Ref : Int J Pharm Compound 2006; 10, 3: 234-236.
02/01/2007 Stability of frozen pemetrexed Pemetrexed is chemically stable for 90 days frozen at -20°C, substantial numbers of microparticulates formes in pemetrexed diluted in the infusion dsolutions in PVC bags upon long-term frozen storage. The avoidance of freezing pemetrexed solutions in PVC bag sis therefore warranted. Ref : Ann Pharmacother 2006 ; 40, 7 : 1289-1292.
29/12/2006 Stability of pemetrexed Pemetrexed 2, 10 and 20 mg/ml is chemically stable for 2 days at room temperature and 31 days refrigerated in dextrose 5% injection and NaCl 0.9% injection. However, substantial numbers of microparticulates may form in pemetrexed diluted in the infusion solutions in PVC bags, especially during longer periods of refrigerated storage. Ref : Ann Pharmacother 2006 ; 40, 6 : 1082-1085.
26/12/2006 Incompatibility furosemide - phenylephrine The solutions of furosemide 4 mg/ml diluted in 5% glucose 5% or 0.9% sodium chloride are incompatible with the solutions of 0.64 mg/ml phenylephrine and 0.4 UI/ml vasopressine. This information is in contradiction with those of Trissel. Ref : Am J Health Syst Pharm 2006 ; 63 : 906-908.
22/12/2006 The website is now translated into 14 languages (Latvian has been included) !
19/12/2006 A new link has been added in the databases towards "Trissel's Calcium & Phosphate Compatibility in Parenteral Nutrition"
14/12/2006
Stability of kétorolac trométhamine Ketorolac tromethamine (Taradyl®) in 5% dextrose infusion may be prepared, frozen in advance by a centralised intravenous admixture service then thawed before use, and the microwave power used for thawing in this study has no impact on the final long-term stability at 4°C at the two concentration (0.1 and 0.3 mg/ml) after 35 days.
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