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开发一种光响应性壳聚糖缀合物前药纳米载体,用于控制 5-氟尿嘧啶抗肿瘤药物的递送。

Development of a photoresponsive chitosan conjugated prodrug nano-carrier for controlled delivery of antitumor drug 5-fluorouracil.

机构信息

Centre for the Environment, Indian Institute of Technology, Guwahati, Assam 781039, India.

Department of Chemistry, Indian Institute of Technology, Guwahati, Assam 781039, India.

出版信息

Int J Biol Macromol. 2019 Jan;121:1070-1076. doi: 10.1016/j.ijbiomac.2018.10.095. Epub 2018 Oct 18.

Abstract

Controlled drug delivery offers improved therapeutic efficacy of the drugs while minimizing side effects. Biocompatible polymers and nanomaterials have emerged as effective carriers for the controlled delivery of drugs. We have synthesized a prodrug of 5-fluorouracil (5FU) covalently conjugated to low molecular weight chitosan (LMWC) via a photocleavable linker. The conjugate was designed to be cleaved under 365 nm UV-A radiations, which is regarded as relatively safe for the cells and release 5FU in a dose-dependent manner. The conjugate showed enhanced water solubility compared to LMWC and forms hydrogel and DMSO gel. The conjugate polymer was also fabricated into nanoparticles by ionic gelation technique. The size of the nanoparticles was found to be in the range 70-90 nm, thus should have the ability to penetrate into living cells. In vitro release study of 5FU from the conjugate showed controlled release of the antitumor drug over time. The synthesized nanoparticles and the gel, therefore, could be a good model for controlled release of antitumor drugs.

摘要

控释给药可提高药物的治疗效果,同时最大限度地减少副作用。生物相容性聚合物和纳米材料已成为药物控释的有效载体。我们通过光可裂解连接子,将 5-氟尿嘧啶(5FU)的前药共价连接到低分子量壳聚糖(LMWC)上。该缀合物旨在在 365nmUV-A 辐射下裂解,这被认为对细胞相对安全,并以剂量依赖性方式释放 5FU。与 LMWC 相比,该缀合物的水溶性得到了提高,并形成水凝胶和 DMSO 凝胶。该缀合物聚合物还通过离子凝胶化技术制成纳米颗粒。发现纳米颗粒的大小在 70-90nm 范围内,因此应该有能力穿透活细胞。从缀合物中释放 5FU 的体外释放研究表明,抗肿瘤药物随时间的释放是可控的。因此,合成的纳米颗粒和凝胶可以作为抗肿瘤药物控释的良好模型。

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