"通过设计提高舌下含服降压药的质量 "的实施情况

IF 2.7 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Deepak Joshi, Naveen K. Choudhary
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引用次数: 0

摘要

背景高血压是一项全球健康挑战,在发达国家和中低收入国家都是导致死亡率和心血管疾病的重要因素。由于舌下腔具有较高的渗透性,因此具有快速吸收药物的潜力,传统的口服片剂往往无法提供急性病症所需的快速起效,这促使人们探索其他非肠道途径。舌下片剂具有生物利用度高、不良反应小和使用方便等优点。然而,配制有效的舌下片剂面临着不同于传统片剂的挑战 QbD 或质量源于设计,是一种有条不紊的制剂开发方法,具有高质量药品、监管灵活性和批准后修改管理等优点。QbD 流程包括定义目标产品的质量特性、了解生产工艺、确定关键材料属性以及优化关键工艺参数。本综述旨在整合有关舌下含服降压药的研究,将系统风险评估方法纳入 QbD 框架。通过应用 QbD 原则优化舌下片剂配方,这种方法有望实现高效的药物产品开发,减少对大量测试的需求,同时确保药物的经济性和有效性。尽管有关舌下片剂的文献综述不胜枚举,但本综述却独树一帜地探讨了在舌下片剂开发中系统实施 QbD 的问题,填补了当前药物研究领域的空白。对关键质量属性的风险识别、分析和评估的探讨,增强了我们对降压药舌下片开发的理解,为制药科学家和研究人员提供了宝贵的资源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

“Implementation of Quality by Design of Sublingual Antihypertensive Drugs"

“Implementation of Quality by Design of Sublingual Antihypertensive Drugs"

Background

Hypertension poses a global health challenge, contributing significantly to mortality and cardiovascular diseases in both developed and low- to middle-income nations. Conventional oral tablets often fail to provide the rapid onset required for acute conditions, prompting exploration of alternative non-parenteral routes.

Main Body

This review focuses on sublingual administration as a viable option, given its potential for rapid drug absorption due to the sublingual cavity's higher permeability. Sublingual tablets offer advantages such as improved bioavailability, minimal adverse effects, and ease of use. However, formulating effective sublingual tablets presents challenges distinct from conventional tablets QbD, or quality by design, is a methodical approach to formulation development., offering benefits like high-quality pharmaceuticals, regulatory flexibility, and post-approval modification management. The QbD process involves defining quality target product profiles, understanding manufacturing processes, identifying critical material attributes, and optimizing key process parameters. This systematic approach ensures a design space that allows for constant improvement throughout the pharmaceutical product lifecycle.

Conclusion

This review aims to consolidate studies on sublingual administration of antihypertensive drugs, incorporating a systematic risk assessment approach within the QbD framework. By applying QbD principles to optimize sublingual tablet formulations, this approach promises efficient drug product development, reducing the need for extensive testing while ensuring affordability and effectiveness. Despite numerous literature reviews on sublingual tablets, this review uniquely addresses the systematic implementation of QbD for sublingual tablet development, filling a gap in the current pharmaceutical research landscape. The exploration of risk identification, analysis, and evaluation of critical quality attributes enhances our understanding of antihypertensive sublingual tablets' development, providing a valuable resource for pharmaceutical scientists and researchers.

Graphical Abstract

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来源期刊
Journal of Pharmaceutical Innovation
Journal of Pharmaceutical Innovation PHARMACOLOGY & PHARMACY-
CiteScore
3.70
自引率
3.80%
发文量
90
审稿时长
>12 weeks
期刊介绍: The Journal of Pharmaceutical Innovation (JPI), is an international, multidisciplinary peer-reviewed scientific journal dedicated to publishing high quality papers emphasizing innovative research and applied technologies within the pharmaceutical and biotechnology industries. JPI''s goal is to be the premier communication vehicle for the critical body of knowledge that is needed for scientific evolution and technical innovation, from R&D to market. Topics will fall under the following categories: Materials science, Product design, Process design, optimization, automation and control, Facilities; Information management, Regulatory policy and strategy, Supply chain developments , Education and professional development, Journal of Pharmaceutical Innovation publishes four issues a year.
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