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首页> 外文期刊>International Journal of Pharmaceutics >Self-implanted tiny needles as alternative to traditional parenteral administrations for controlled transdermal drug delivery
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Self-implanted tiny needles as alternative to traditional parenteral administrations for controlled transdermal drug delivery

机译:自植入微小针作为传统肠胃外给药的替代,用于控制透皮药物递送

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摘要

Controlled drug-delivery systems have potential as substitutes for traditional medication systems due to the advantages in safety, efficacy, and patient compliance that these long-acting dosage forms provide. In this context, the present study focus on the development of self-implanted hyaluronic acid (HA) tiny needles that encapsulate ivermectin (IVM)-poly (lactic-co-glycolic acid) (PLGA) microparticles for controlled transdermal IVM release to treat parasitic diseases. The fabricated tiny needles involved matching portable applicator have potentially able for self-administration by patients without intense pain or complexity of current controlled-release devices. The biodegradable IVM-loaded PLGA microparticles were prepared and encapsulated within the tip of dissolving HA tiny needles to achieve high delivery efficiency. The drug loading of tiny needles might be controlled by varying the repeat time of filling or pressing processes. In-vitro tests showed that the tiny needles have sufficient mechanical strength to be inserted into skin within seconds and, next rapidly dissolved to release the loaded drug carriers into subcutaneous tissues for intradermal sustained IVM release. With the in-vivo test in rats, the insertion site recovered barrier property within 3 h. In comparison to traditional hypodermic injection or implantation of controlled-release systems, the proposed polymer tiny needles can be considered as a promising device for controlled transdermal drug delivery.
机译:由于安全性,疗效和患者符合性的优点,受控药物输送系统具有用于传统药物系统的替代品。在这种情况下,本研究重点是自植入透明质酸(HA)微小针的发展,该透明质酸(HA)微小针封装Ivermectin(IVM)-poly(乳酸 - 共乙醇酸)(PLGA)微粒用于控制的透皮IVM释放以治疗寄生疾病。涉及匹配的便携式涂抹器的制造的微小针潜在能够通过无强烈疼痛或复杂性的患者自我管理的患者。制备可生物降解的IVM负载的PLGA微粒,并封装在溶解HA微小针头的尖端内,以实现高输送效率。通过改变填充或压制过程的重复时间来控制微小针的药物负荷。在体外测试表明,微小针具有足够的机械强度,以在几秒钟内插入皮肤中,然后迅速溶解,以将负载的药物载体释放到皮下组织中,用于皮内组织用于皮内持续的IVM释放。随着大鼠的体内试验,插入位点在3小时内回收阻隔性。与传统的皮肤注射或受控释放系统的植入相比,所提出的聚合物微小针可以被认为是受控透皮药物递送的有希望的装置。

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