Gastroretentive microballoons of olmesartan medoxomil: formulation and in vitro-in vivo evaluation.

IF 2.2 Q2 PHARMACOLOGY & PHARMACY Therapeutic delivery Pub Date : 2025-03-01 Epub Date: 2025-02-25 DOI:10.1080/20415990.2025.2466418
Archana S Patil, Shweta Aloshi, Yadishma Gaude, Rajashree S Masareddy
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Abstract

Background: Olmesartan medoxomil, classified as BCS class II due to its poor water solubility, exhibits a low oral bioavailability of 28.6%.

Materials and methods: Microballoons of Olmesartan medoxomil were formulated using the ionotropic gelation technique and subjected to various evaluation parameters.

Results: The particles were found to be in the range of 85.11 to 312.6 µm. The prepared microballoons remained buSSoyant for more than 12 hours and showed percentage of cumulative drug release between 56.32-83.62%. In vivo studies showed significant reduction in Systolic blood pressure (SBP) in optimized formulation (OF).

Conclusion: The formulated microballoons (hollow microspheres) emerged as a promising option for an oral gastro retentive controlled drug delivery system for Olmesartan medoxomil.

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奥美沙坦美多索米胃保留微球:配方及体内外评价。
背景:奥美沙坦美多索米因其水溶性较差,被列为BCS II类药物,其口服生物利用度较低,为28.6%。材料与方法:采用离子化凝胶法制备了奥美沙坦美多沙密微球,并对其进行了各种评价参数的测定。结果:所得颗粒粒径范围为85.11 ~ 312.6µm。制备的微球在bussoant中停留时间超过12小时,累积释药率在56.32 ~ 83.62%之间。体内研究表明,优化配方(OF)可显著降低收缩压(SBP)。结论:所制备的微球(空心微球)是一种很有前途的口服胃内给药系统。
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来源期刊
Therapeutic delivery
Therapeutic delivery PHARMACOLOGY & PHARMACY-
CiteScore
5.50
自引率
0.00%
发文量
25
期刊介绍: Delivering therapeutics in a way that is right for the patient - safe, painless, reliable, targeted, efficient and cost effective - is the fundamental aim of scientists working in this area. Correspondingly, this evolving field has already yielded a diversity of delivery methods, including injectors, controlled release formulations, drug eluting implants and transdermal patches. Rapid technological advances and the desire to improve the efficacy and safety profile of existing medications by specific targeting to the site of action, combined with the drive to improve patient compliance, continue to fuel rapid research progress. Furthermore, the emergence of cell-based therapeutics and biopharmaceuticals such as proteins, peptides and nucleotides presents scientists with new and exciting challenges for the application of therapeutic delivery science and technology. Successful delivery strategies increasingly rely upon collaboration across a diversity of fields, including biology, chemistry, pharmacology, nanotechnology, physiology, materials science and engineering. Therapeutic Delivery recognizes the importance of this diverse research platform and encourages the publication of articles that reflect the highly interdisciplinary nature of the field. In a highly competitive industry, Therapeutic Delivery provides the busy researcher with a forum for the rapid publication of original research and critical reviews of all the latest relevant and significant developments, and focuses on how the technological, pharmacological, clinical and physiological aspects come together to successfully deliver modern therapeutics to patients. The journal delivers this essential information in concise, at-a-glance article formats that are readily accessible to the full spectrum of therapeutic delivery researchers.
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