Author:
Farag Michael M.,Louis Mina M.,Badawy Alia A.,Nessem Demiana I.,Elmalak Nevine S. Abd
Abstract
AbstractThis study aims to prepare drotaverine hydrochloride superporous hydrogel hybrid systems (DSHH systems) to prolong its residence time in the stomach, provide extended release and reduce its frequency of administration. Drotaverine hydrochloride (DRH) is a spasmolytic drug that suffers from brief residence due to intestinal hypermotility during diarrheal episodes associated with gastrointestinal colics resulting in low bioavailability and repeated dosing. Eight DSHH systems were prepared using gas blowing technique. The prepared DSHH systems were evaluated regarding their morphology, incorporation efficiency, density, porosity, swelling ratio, viscoelastic property, erosion percentage and release kinetics. The FH8 formula containing equal proportion of chitosan (3%) /polyvinyl alcohol (3%) as strengthener and crosslinked with tripolyphosphate showed the highest incorporation efficiency (91.83 ± 1.33%), good swelling ratio (28.32 ± 3.15% after 24 h), optimum viscoelastic properties (60.19 ± 3.82 kPa) and sustained release profile (88.03 ± 2.15% after 24 h). A bioequivalence study was done to compare the bioavailability of the candidate formula versus Spasmocure®. Statistical analysis showed significant (P < 0.05) increase in bioavailability 2.7 folds with doubled Tmax (4 h) compared to the marketed product (2 h). These results declared that the superporous hydrogel hybrid systems could be a potential gastroretentive approach for the sustained delivery of drugs with short residence time with enhanced viscoelasticity.
Graphical abstract
Publisher
Springer Science and Business Media LLC
Subject
Drug Discovery,Pharmaceutical Science,Agronomy and Crop Science,Ecology,Aquatic Science,General Medicine,Ecology, Evolution, Behavior and Systematics
Reference63 articles.
1. Kumar D, Kumar A, Malik JK. Preformulation studies of drotaverine hydrochloride: an integral part of formulation design. European Journal of Biomedical and Pharmaceutical Sciences. 2019;6(13):304–7.
2. Mehmood Y, Mahmood RK, Akram W. Development and validation of UV-spectrophotometric methods for quantitative estimation of drotaverine HCl injection. Pharm Methods. 2017;8(1):31–5.
3. Patel P, Dand N, Somwanshi A, Kadam VJ, Hirlekar RS. Design and evaluation of a sustained release gastroretentive dosage form of captopril: a technical note. AAPS PharmSciTech. 2008;9(3):836–9.
4. Kushal M, Monali M, Durgavati M, Mittal P, Umesh S, Pragna S. Oral controlled release drug delivery system: an overview. Int Res J Pharm. 2013;4(3):70–6.
5. Kumar S, Jamil F, Rajput M, Sharma S. Gastro Retentive Drug Delivery System : Features and Facts. Int J Res Pharm Biomed Sci. 2012;3(1):125–36.
Cited by
4 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献