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Injectable visible light-cured glycol chitosan hydrogels with controlled release of anticancer drugs for local cancer therapy in vivo: a feasible study

机译:可注射可见的光固化二醇壳聚糖壳聚糖水凝胶,用于体内局部癌症治疗的抗癌药物的控制释放:可行的研究

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摘要

Currently available chemotherapy is associated with serious side effects, and therefore novel drug delivery systems (DDSs) are required to specifically deliver anticancer drugs to targeted sites. In this study, we evaluated the feasibility of visible light-cured glycol chitosan (GC) hydrogels with controlled release of doxorubicinhydrochloride (DOXHCl) as local DDSs for effective cancer therapy in vivo. The storage modulus of the hydrogel precursor solutions was increased as a function of visible light irradiation time. In addition, the swelling ratio of the hydrogel irradiated for 10s (GC(10)/DOX) was greater than in 60s (GC(60)/DOX). In vitro release test showed that DOX was rapidly released in GC(10)/DOX compared with GC(60)/DOX due to the density of cross-linking. In vitro and in vivo tests including cell viability and measurement of tumor volume showed that the local treatment of GC(10)/DOX yielded substantially greater antitumor effect compared with that of GC(60)/DOX. Therefore, the visible light-cured GC hydrogel system may exhibit clinical potential as a local DDS of anticancer drugs with controlled release, by modulating cross-linking density.
机译:目前可用的化疗与严重的副作用有关,因此需要新的药物递送系统(DDS)来特异性将抗癌药物递给靶向位点。在该研究中,我们评估了可见光甘油壳聚糖(GC)水凝胶的可行性,使多柔霉盐(DOXHCL)的控制释放作为局部DDS的体内有效癌症治疗。随着可见光照射时间的函数,水凝胶前体溶液的储存模量增加。另外,辐照10S的水凝胶的溶胀比(GC(10)/ dox)大于60s(GC(60)/ dox)。体外释放试验表明,由于交联密度,与GC(60)/ DOX相比,在GC(10)/ dox中快速释放DOX。体外和体内试验包括细胞活力和肿瘤体积的测量表明,与GC(60)/ dox的GC(60)/ dox相比,GC(10)/ dox的局部处理基本更大的抗肿瘤效应。因此,通过调节交联密度,可见光固化的GC水凝胶系统可以表现为具有受控释放的抗癌药物的局部DDS的临床电位。

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