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支化型乙烯基吡咯烷酮共聚物作为亲水性生物活性化合物载体的结构和状态。

Structure and State of Water in Branched -Vinylpyrrolidone Copolymers as Carriers of a Hydrophilic Biologically Active Compound.

机构信息

Institute of Problems of Chemical Physics, Russian Academy of Sciences, Prosp. Akad. Semenova 1, 142432 Chernogolovka, Russia.

Department of Fundamental Physical and Chemical Engineering, M.V. Lomonosov Moscow State University, Leninskie Gory 1, 119991 Moscow, Russia.

出版信息

Molecules. 2020 Dec 18;25(24):6015. doi: 10.3390/molecules25246015.

DOI:10.3390/molecules25246015
PMID:33353192
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7765915/
Abstract

Hydrated copolymers of -vinylpyrrolidone (VP) with triethylene glycol dimethacrylate as a promising platform for biologically active compounds (BAC) were investigated by different physical chemical methods (dynamic light scattering, infrared spectroscopy, thermal gravimetric analysis, and differential scanning calorimetry) and the quantum chemical modeling of water coordination by the copolymers in a solution. According to the quantum chemical simulation, one to two water molecules can coordinate on one O-atom of the lactam ring of VP units in the copolymer. Besides the usual terminal coordination, the water molecule can form bridges to bind two adjacent C=O groups of the lactam rings of VP units. In addition to the first hydration shell, the formation of a second one is also possible due to the chain addition of water molecules, and its structure depends on a mutual orientation of C=O groups. We showed that ,-dimethylbiguanidine hydrochloride (metformin) as a frontline drug for the treatment of type 2 diabetes mellitus can be associated in aqueous solutions with free and hydrated C=O groups of the lactam rings of VP units in studied copolymers. Based on the characteristics of the H-bonds, we believe that the level of the copolymer hydration does not affect the behavior and biological activity of this drug, but the binding of metformin with the amphiphilic copolymer will delight in the penetration of a hydrophilic drug across a cell membrane to increase its bioavailability.

摘要
  • 乙烯基吡咯烷酮(VP)与三乙二醇二甲基丙烯酸酯的水合共聚物作为生物活性化合物(BAC)的有前途的平台,通过不同的物理化学方法(动态光散射、红外光谱、热重分析和差示扫描量热法)进行了研究,并通过量子化学建模研究了共聚物在溶液中对水的配位。根据量子化学模拟,一个到两个水分子可以在共聚物中 VP 单元的内酰胺环的一个 O 原子上配位。除了通常的末端配位外,水分子还可以形成桥,将 VP 单元的内酰胺环的两个相邻的 C=O 基团连接起来。除了第一水合壳外,由于水分子的链加成,还可能形成第二个水合壳,其结构取决于 C=O 基团的相互取向。我们表明,盐酸二甲双胍(二甲双胍)作为治疗 2 型糖尿病的一线药物,可以在水溶液中与研究共聚物中 VP 单元内酰胺环的游离和水合 C=O 基团结合。基于氢键的特点,我们认为共聚物的水合程度不会影响这种药物的行为和生物活性,但二甲双胍与两亲共聚物的结合将有助于亲水性药物穿过细胞膜渗透,从而提高其生物利用度。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da1/7765915/1df55e15b532/molecules-25-06015-g010a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da1/7765915/5a1fa020cd0b/molecules-25-06015-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da1/7765915/a3aafb09d2c5/molecules-25-06015-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da1/7765915/61279ddfc429/molecules-25-06015-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da1/7765915/f9ca3b2c632c/molecules-25-06015-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da1/7765915/99137e2d4028/molecules-25-06015-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da1/7765915/7f59876ace41/molecules-25-06015-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da1/7765915/47739e4536c9/molecules-25-06015-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da1/7765915/e94d3c30a3ba/molecules-25-06015-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da1/7765915/2638573d1766/molecules-25-06015-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da1/7765915/7d6366212076/molecules-25-06015-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da1/7765915/a8fef08df6b1/molecules-25-06015-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da1/7765915/1df55e15b532/molecules-25-06015-g010a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da1/7765915/5a1fa020cd0b/molecules-25-06015-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da1/7765915/a3aafb09d2c5/molecules-25-06015-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da1/7765915/61279ddfc429/molecules-25-06015-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da1/7765915/f9ca3b2c632c/molecules-25-06015-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da1/7765915/99137e2d4028/molecules-25-06015-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da1/7765915/7f59876ace41/molecules-25-06015-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da1/7765915/47739e4536c9/molecules-25-06015-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da1/7765915/e94d3c30a3ba/molecules-25-06015-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da1/7765915/2638573d1766/molecules-25-06015-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da1/7765915/7d6366212076/molecules-25-06015-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da1/7765915/a8fef08df6b1/molecules-25-06015-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da1/7765915/1df55e15b532/molecules-25-06015-g010a.jpg

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