局麻药缓释系统在疼痛治疗中的应用进展。

IF 6.5 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Drug Delivery Pub Date : 2024-12-01 Epub Date: 2023-12-21 DOI:10.1080/10717544.2023.2296349
Yulu Chen, Jingmei Xu, Ping Li, Liyang Shi, Sha Zhang, Qulian Guo, Yong Yang
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引用次数: 0

摘要

疼痛治疗仍然是当今最常见的临床问题之一,但在很大程度上尚未得到解决。局麻药在疼痛治疗中发挥着不可或缺的作用。传统局麻药的主要局限性在于单次注射的持续时间有限。为解决这一问题,临床上通常会放置导管或与其他药物联合使用,以延长局麻药的作用时间。然而,这种方法并不能满足临床镇痛的需要。因此,许多研究人员致力于开发可单次给药的局麻药缓释类型。近年来,药物缓释系统因其持续时间长、疗效好等特点而异军突起,为局麻药的应用提供了更多可能。本文总结了局麻药给药系统的类型及其临床应用,结合局麻药的相关研究进行了讨论,并对局麻药缓释剂的发展进行了总结和展望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Advances in the use of local anesthetic extended-release systems in pain management.

Pain management remains among the most common and largely unmet clinical problems today. Local anesthetics play an indispensable role in pain management. The main limitation of traditional local anesthetics is the limited duration of a single injection. To address this problem, catheters are often placed or combined with other drugs in clinical practice to increase the time that local anesthetics act. However, this method does not meet the needs of clinical analgesics. Therefore, many researchers have worked to develop local anesthetic extended-release types that can be administered in a single dose. In recent years, drug extended-release systems have emerged dramatically due to their long duration and efficacy, providing more possibilities for the application of local anesthetics. This paper summarizes the types of local anesthetic drug delivery systems and their clinical applications, discusses them in the context of relevant studies on local anesthetics, and provides a summary and outlook on the development of local anesthetic extended-release agents.

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来源期刊
Drug Delivery
Drug Delivery 医学-药学
CiteScore
11.80
自引率
5.00%
发文量
250
审稿时长
3.3 months
期刊介绍: Drug Delivery is an open access journal serving the academic and industrial communities with peer reviewed coverage of basic research, development, and application principles of drug delivery and targeting at molecular, cellular, and higher levels. Topics covered include all delivery systems including oral, pulmonary, nasal, parenteral and transdermal, and modes of entry such as controlled release systems; microcapsules, liposomes, vesicles, and macromolecular conjugates; antibody targeting; protein/peptide delivery; DNA, oligonucleotide and siRNA delivery. Papers on drug dosage forms and their optimization will not be considered unless they directly relate to the original drug delivery issues. Published articles present original research and critical reviews.
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