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自组装的乙二醇壳聚糖纳米凝胶,含有棕榈酰化的 exendin-4 肽,作为长效抗糖尿病吸入系统。

Self-assembled glycol chitosan nanogels containing palmityl-acylated exendin-4 peptide as a long-acting anti-diabetic inhalation system.

机构信息

College of Pharmacy, Pusan National University, Jangjeon-dong, Geumjeong-gu, Busan 609-735, Republic of Korea.

出版信息

J Control Release. 2012 Aug 10;161(3):728-34. doi: 10.1016/j.jconrel.2012.05.029. Epub 2012 May 22.

Abstract

Inhalable deoxycholic acid-modified glycol chitosan (DOCA-GC) nanogels containing palmityl acylated exendin-4 (Ex4-C16) were prepared by self-assembly and characterized physicochemically. The lung deposition of DOCA-GC nanogels was monitored using an infrared imaging system, and the hypoglycemia caused by Ex4-C16-loaded DOCA-GC nanogels was evaluated after pulmonary administration in type 2 diabetic db/db mice. The cytotoxicities and lung histologies induced by DOCA-GC nanogels were examined in human lung epithelial cells (A549 and Calu-3) and db/db mice, respectively. Results showed that the DOCA-GC nanogels prepared were spherical and compact and had a diameter of ~220 nm. Although the incorporation of Ex4-C16 (50.9±7.8%) into DOCA-GC nanogels was significantly lower than that of Ex4 (81.4±4.9%), the Ex4-C16 release from DOCA-GC nanogels was greatly delayed vs. Ex4. DOCA-GC nanogels were deposited rapidly after pulmonary administration and remained in the lungs for ~72 h. Furthermore, the hypoglycemic duration of inhaled Ex4-C16 nanogels was much greater than that of Ex4 nanogels in db/db mice. Cytotoxicity results of DOCA-GC nanogels were considered acceptable, and the tissue histologies of mouse lungs administered nanogels did not show any significant difference vs. control lungs. The authors believe that Ex4-C16 DOCA-GC nanogels offer a long-acting inhalation delivery system for treating type 2 diabetes.

摘要

可吸入脱胆酸修饰的乙二醇壳聚糖(DOCA-GC)纳米凝胶载棕榈酰化 Exendin-4(Ex4-C16)通过自组装制备,并进行理化性质表征。使用红外成像系统监测 DOCA-GC 纳米凝胶的肺部沉积情况,并在 2 型糖尿病 db/db 小鼠中通过肺部给药评估载有 Ex4-C16 的 DOCA-GC 纳米凝胶引起的低血糖。在人肺上皮细胞(A549 和 Calu-3)和 db/db 小鼠中,分别检查了 DOCA-GC 纳米凝胶的细胞毒性和肺部组织学。结果表明,所制备的 DOCA-GC 纳米凝胶呈球形且致密,直径约为 220nm。尽管 Ex4-C16(50.9±7.8%)掺入 DOCA-GC 纳米凝胶的比例明显低于 Ex4(81.4±4.9%),但与 Ex4 相比,Ex4-C16 从 DOCA-GC 纳米凝胶中的释放大大延迟。DOCA-GC 纳米凝胶给药后肺部迅速沉积,并在肺部停留约 72 小时。此外,吸入的 Ex4-C16 纳米凝胶的降血糖持续时间比 db/db 小鼠中吸入的 Ex4 纳米凝胶长得多。DOCA-GC 纳米凝胶的细胞毒性结果被认为是可以接受的,并且给予纳米凝胶的小鼠肺部组织学与对照肺部没有任何显著差异。作者认为,Ex4-C16 DOCA-GC 纳米凝胶为治疗 2 型糖尿病提供了一种长效吸入给药系统。

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