Effect of intra- and extragranular addition of highly porous tribasic calcium phosphate on properties of immediate release acyclovir formulation – Comparison with commercial tablets using compendial and biorelevant dissolution methods
暂无分享,去创建一个
[1] Parind Mahendrakumar Desai,et al. Review of Disintegrants and the Disintegration Phenomena. , 2016, Journal of pharmaceutical sciences.
[2] Kishore Kumar Hotha,et al. Drug-Excipient Interactions: Case Studies and Overview of Drug Degradation Pathways , 2016 .
[3] P. Langguth,et al. Oral Solid Dosage Form Disintegration Testing - The Forgotten Test. , 2015, Journal of pharmaceutical sciences.
[4] Mario A. González,et al. The Effect of Excipients on the Permeability of BCS Class III Compounds and Implications for Biowaivers , 2015, Pharmaceutical Research.
[5] Juraj Sibik,et al. The Disintegration Process in Microcrystalline Cellulose Based Tablets, Part 1: Influence of Temperature, Porosity and Superdisintegrants , 2015, Journal of pharmaceutical sciences.
[6] Peter Kleinebudde,et al. A critical review on tablet disintegration , 2015, Pharmaceutical development and technology.
[7] K. Kamiński,et al. The Improvement of the Dissolution Rate of Ziprasidone Free Base from Solid Oral Formulations , 2015, AAPS PharmSciTech.
[8] W. Weitschies,et al. A biorelevant dissolution stress test device – background and experiences , 2010, Expert opinion on drug delivery.
[9] Werner Weitschies,et al. Investigation of dissolution behavior of diclofenac sodium extended release formulations under standard and biorelevant test conditions , 2010, Drug development and industrial pharmacy.
[10] M. Roberts,et al. Compatibility studies of acyclovir and lactose in physical mixtures and commercial tablets. , 2009, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[11] Bertil Abrahamsson,et al. Comparison of dissolution profiles obtained from nifedipine extended release once a day products using different dissolution test apparatuses. , 2009, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[12] M. Khan,et al. Disintegration of Highly Soluble Immediate Release Tablets: A Surrogate for Dissolution , 2009, AAPS PharmSciTech.
[13] D. Barends,et al. Biowaiver monographs for immediate release solid oral dosage forms: aciclovir. , 2008, Journal of pharmaceutical sciences.
[14] Clive G. Wilson,et al. Irregular absorption profiles observed from diclofenac extended release tablets can be predicted using a dissolution test apparatus that mimics in vivo physical stresses. , 2008, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[15] D. Barends,et al. Biowaiver monographs for immediate release solid oral dosage forms: ethambutol dihydrochloride. , 2008, Journal of pharmaceutical sciences.
[16] D M Barends,et al. Biowaiver monographs for immediate release solid oral dosage forms: ranitidine hydrochloride. , 2005, Journal of pharmaceutical sciences.
[17] D. Barends,et al. Biowaiver monographs for immediate release solid oral dosage forms based on biopharmaceutics classification system (BCS) literature data: verapamil hydrochloride, propranolol hydrochloride, and atenolol. , 2004, Journal of pharmaceutical sciences.
[18] B. Guglielmo,et al. Pharmacokinetics of valaciclovir. , 2004, The Journal of antimicrobial chemotherapy.
[19] Sarfaraz K. Niazi. Waiver of In Vivo Bioavailability and Bioequivalence Studies for Immediate-Release Solid Oral Dosage Forms Based on a Biopharmaceutics Classification System , 2004, Handbook of Pharmaceutical Manufacturing Formulations, Third Edition.
[20] Michael Levin. Waiver of In Vivo Bioavailability and Bioequivalence Studies for Immediate-Release Solid Oral Dosage Forms Based on a Biopharmaceutics Classification System , 2001 .
[21] G L Amidon,et al. A compartmental absorption and transit model for estimating oral drug absorption. , 1999, International journal of pharmaceutics.
[22] M. Georgarakis,et al. Acyclovir serum concentrations following peroral administration of magnetic depot tablets and the influence of extracorporal magnets to control gastrointestinal transit. , 1998, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[23] Lawrence X. Yu,et al. Compartmental transit and dispersion model analysis of small intestinal transit flow in humans , 1996 .
[24] M S Gordon,et al. Effect of the mode of super disintegrant incorporation on dissolution in wet granulated tablets. , 1993, Journal of pharmaceutical sciences.
[25] Raoul Kopelman,et al. Fractal Reaction Kinetics , 1988, Science.
[26] L. Lewis,et al. Human gastrointestinal absorption of acyclovir from tablet duodenal infusion and sipped solution. , 1986, British journal of clinical pharmacology.
[27] G. K. Bolhuis,et al. Improvement by super disintegrants of the properties of tablets containing lactose, prepared by wet granulation , 1983, Pharmaceutisch Weekblad.
[28] O. Laskin. Clinical Pharmacokinetics of Acyclovir , 1983, Clinical pharmacokinetics.
[29] E. Shotton,et al. The effect of intra‐ and extragranular maize starch on the disintegration of compressed tablets , 1972, The Journal of pharmacy and pharmacology.
[30] J. Gajdziok. Superdisintegrants used in pharmaceutical technology. , 2019, Ceska a Slovenska farmacie : casopis Ceske farmaceuticke spolecnosti a Slovenske farmaceuticke spolecnosti.
[31] D. Zakowiecki,et al. Beyond just a filler – application of calcium phosphates in direct compression formulations-BPD , 2018 .
[32] S. Jain,et al. APPROACHES FOR ENHANCING THE BIOAVAILABILITY OF ACYCLOVIR: A CRITICAL REVIEW , 2013 .
[33] Y. Qiu,et al. Understanding Drug Properties in Formulation and Process Design of Solid Oral Products , 2010 .
[34] Sarsvatkumar Patel,et al. Compression physics in the formulation development of tablets. , 2006, Critical reviews in therapeutic drug carrier systems.
[35] L L Augsburger,et al. The role of intra- and extragranular microcrystalline cellulose in tablet dissolution. , 1996, Pharmaceutical development and technology.