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用于快速高效局部麻醉的载利多卡因溶解微针的研发。

Development of Lidocaine-Loaded Dissolving Microneedle for Rapid and Efficient Local Anesthesia.

作者信息

Yang Huisuk, Kang Geonwoo, Jang Mingyu, Um Daniel Junmin, Shin Jiwoo, Kim Hyeonjun, Hong Jintae, Jung Hyunji, Ahn Hyemyoung, Gong Seongdae, Lee Chisong, Jung Ui-Won, Jung Hyungil

机构信息

JUVIC Inc., No. 208, Digital-ro 272, Guro-gu, Seoul 08389, Korea.

Department of Biotechnology, Building 123, Yonsei University, 50 Yonsei-ro, Seodaemun-gu, Seoul 03722, Korea.

出版信息

Pharmaceutics. 2020 Nov 9;12(11):1067. doi: 10.3390/pharmaceutics12111067.

DOI:10.3390/pharmaceutics12111067
PMID:33182374
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7695299/
Abstract

Lidocaine is a local anesthetic agent used in the form of injection and topical cream. However, these formulation types have limitations of being either painful or slow-acting, thereby hindering effective and complete clinical performance of lidocaine. Dissolving microneedles (DMNs) are used to overcome these limitations owing to their fast onset time and minimally invasive administration methods. Using hyaluronic acid and lidocaine to produce the drug solution, a lidocaine HCl encapsulated DMN (Li-DMN) was fabricated by centrifugal lithography. The drug delivery rate and local anesthetic quality of Li-DMNs were evaluated using the pig cadaver insertion test and Von Frey behavior test. Results showed that Li-DMNs could deliver sufficient lidocaine for anesthesia that is required to be utilized for clinical level. Results from the von Frey test showed that the anesthetic effect of Li-DMNs was observed within 10 min after administration, thus confirming fast onset time. A toxicity test for appropriate clinical application standard was conducted with a microbial limit test and an animal skin irritation test, showing absence of skin irritation and irritation-related microorganisms. Overall, Li-DMN is a possible alternative drug delivery method for local anesthesia, meeting the requirements for clinical conditions and overcoming the drawbacks of other conventional lidocaine administration methods.

摘要

利多卡因是一种以注射剂和外用乳膏形式使用的局部麻醉剂。然而,这些剂型存在疼痛或起效缓慢的局限性,从而阻碍了利多卡因的有效和完整临床应用。溶解微针(DMNs)因其起效时间快和给药方式微创而被用于克服这些局限性。利用透明质酸和利多卡因制备药物溶液,通过离心光刻法制备了盐酸利多卡因包封的微针(Li-DMN)。使用猪尸体插入试验和von Frey行为试验评估了Li-DMN的药物递送率和局部麻醉质量。结果表明,Li-DMN能够递送足够的利多卡因用于临床水平所需的麻醉。von Frey试验结果表明,给药后10分钟内观察到Li-DMN的麻醉效果,从而证实了起效时间快。通过微生物限度试验和动物皮肤刺激性试验进行了符合适当临床应用标准的毒性试验,结果显示无皮肤刺激和与刺激相关的微生物。总体而言,Li-DMN是一种可能的局部麻醉药物递送替代方法,满足临床条件要求并克服了其他传统利多卡因给药方法的缺点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0fa/7695299/88f7b8a53fa7/pharmaceutics-12-01067-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0fa/7695299/ea534731c86a/pharmaceutics-12-01067-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0fa/7695299/e3c6ab4e2af5/pharmaceutics-12-01067-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0fa/7695299/544ec7aa602e/pharmaceutics-12-01067-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0fa/7695299/f5769a4709bf/pharmaceutics-12-01067-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0fa/7695299/fa02158e713c/pharmaceutics-12-01067-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0fa/7695299/88f7b8a53fa7/pharmaceutics-12-01067-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0fa/7695299/ea534731c86a/pharmaceutics-12-01067-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0fa/7695299/e3c6ab4e2af5/pharmaceutics-12-01067-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0fa/7695299/544ec7aa602e/pharmaceutics-12-01067-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0fa/7695299/f5769a4709bf/pharmaceutics-12-01067-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0fa/7695299/fa02158e713c/pharmaceutics-12-01067-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0fa/7695299/88f7b8a53fa7/pharmaceutics-12-01067-g006.jpg

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本文引用的文献

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