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基于(林奈)加尔特纳多糖的纳米凝胶的构建与性能评估。

Construction and Performance Evaluation of (Linn.) Gaertn. Polysaccharide-Based Nanogel.

作者信息

Liu Fangyan, Shen Chen, Chen Xuelian, Gao Fei, Chen Yin

机构信息

College of Food and Pharmacy, Zhejiang Ocean University, Zhoushan 316000, China.

出版信息

Polymers (Basel). 2023 Apr 19;15(8):1933. doi: 10.3390/polym15081933.

DOI:10.3390/polym15081933
PMID:37112079
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10143989/
Abstract

The nanogels made from these polysaccharides and their derivatives are often used to construct drug delivery systems owing to their biocompatible, biodegradable, non-toxic, water-soluble, and bioactive characteristics. In this work, a novel pectin with unique gelling properties was extracted from the seed of (NPGP). The structural research indicated that NPGP was a low methoxyl pectin with a high content of galacturonic acid. NPGP-based nanogels (NGs) were accomplished employing the water in oil (W/O) nano-emulsion method. The cysteamine containing reduction-responsive bond and integrin-targeting RGD peptide were also grafted onto NPGP. The anti-tumor drug doxorubicin hydrochloride (DOX) was loaded during the formation of NGs, and the performance of DOX delivery was studied. The NGs were characterized by UV-vis, DLS, TEM, FT-IR, and XPS. The results showed that the prepared NGs were nanosized (167.6 ± 53.86 nm), had excellent encapsulation efficiency (91.61 ± 0.85%), and possessed a fine drug loading capacity (8.40 ± 0.16%). The drug release experiment showed that DOX@NPGP-SS-RGD had good redox-responsive performance. Furthermore, the results of cell experiments revealed good biocompatibility of prepared NGs, along with selective absorption by HCT-116 cells through integrin receptor-mediated endocytosis to play an anti-tumor effect. These studies indicated the potential application of NPGP-based NGs as targeted drug delivery systems.

摘要

由这些多糖及其衍生物制成的纳米凝胶,因其具有生物相容性、可生物降解、无毒、水溶性和生物活性等特性,常被用于构建药物递送系统。在本研究中,从[具体植物名称]种子中提取了一种具有独特胶凝特性的新型果胶(NPGP)。结构研究表明,NPGP是一种半乳糖醛酸含量高的低甲氧基果胶。采用油包水(W/O)纳米乳液法制备了基于NPGP的纳米凝胶(NGs)。还将含有还原响应键的半胱胺和整合素靶向RGD肽接枝到NPGP上。在NGs形成过程中负载抗肿瘤药物盐酸阿霉素(DOX),并研究了DOX的递送性能。通过紫外可见光谱、动态光散射、透射电子显微镜、傅里叶变换红外光谱和X射线光电子能谱对NGs进行了表征。结果表明,所制备的NGs为纳米尺寸(167.6±53.86 nm),具有优异的包封率(91.61±0.85%)和良好的载药能力(8.40±0.16%)。药物释放实验表明,DOX@NPGP-SS-RGD具有良好的氧化还原响应性能。此外,细胞实验结果显示所制备的NGs具有良好的生物相容性,并且HCT-116细胞通过整合素受体介导的内吞作用进行选择性吸收,从而发挥抗肿瘤作用。这些研究表明基于NPGP的NGs作为靶向药物递送系统具有潜在的应用价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b5f/10143989/d548a371342a/polymers-15-01933-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b5f/10143989/ef9f79acf32b/polymers-15-01933-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b5f/10143989/c09d8b6c96a1/polymers-15-01933-g001a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b5f/10143989/25f7765c7557/polymers-15-01933-g002a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b5f/10143989/f7c5dc622b5b/polymers-15-01933-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b5f/10143989/452027621dca/polymers-15-01933-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b5f/10143989/d548a371342a/polymers-15-01933-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b5f/10143989/ef9f79acf32b/polymers-15-01933-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b5f/10143989/c09d8b6c96a1/polymers-15-01933-g001a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b5f/10143989/25f7765c7557/polymers-15-01933-g002a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b5f/10143989/f7c5dc622b5b/polymers-15-01933-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b5f/10143989/452027621dca/polymers-15-01933-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b5f/10143989/d548a371342a/polymers-15-01933-g005.jpg

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