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利用流体动力肢体静脉注射的中性嵌段共聚物辅助基因传递。

Neutral Block Copolymer Assisted Gene Delivery using Hydrodynamic Limb Vein Injection.

机构信息

Univ Brest, INSERM, EFS, UMR 1078, GGB-GTCA Team, Brest, F-29200, France.

CHU de Brest, Service de Génétique Médicale et de Biologie de la Reproduction, Centre de Référence des Maladies Rares Maladies Neuromusculaires, Brest, 29200, France.

出版信息

Macromol Biosci. 2024 Jul;24(7):e2300568. doi: 10.1002/mabi.202300568. Epub 2024 Mar 29.

Abstract

Three different amphiphilic block copolymer families are synthesized to investigate new opportunities to enhance gene delivery via Hydrodynamic Limb Vein (HLV) injections. First a polyoxazoline-based family containing mostly one poly(2-methyl-2-oxazoline) (PMeOx) block and a second block POx with an ethyl (EtOx), isopropyl (iPrOx) or phenyl substituent (PhOx) is synthesized. Then an ABC poly(2-ethyl-2-oxazoline)-b-poly(2-n-propyl-2-oxazoline)-b-poly(2-methyl-2-oxazoline) triblock copolymer is synthesized, with a thermosensitive middle block. Finally, polyglycidol-b-polybutylenoxide-b-polyglycidol copolymers with various molar masses and amphiphilic balance are produced. The simple architecture of neutral amphiphilic triblock copolymer is not sufficient to obtain enhanced in vivo gene transfection. Double or triple amphiphilic neutral block copolymers are improving the in vivo transfection performances through HLV administration as far as a block having an lower critical solution temperature is incorporated in the vector. The molar mass of the copolymer does not seem to affect the vector performances in a significant manner.

摘要

三种不同的两亲性嵌段共聚物家族被合成,以探索通过血流动力学肢体静脉(HLV)注射增强基因传递的新机会。首先合成了一种基于聚恶唑啉的家族,该家族主要包含一个聚(2-甲基-2-恶唑啉)(PMeOx)嵌段和一个具有乙基(EtOx)、异丙基(iPrOx)或苯基取代基(PhOx)的第二个 POx 嵌段。然后合成了一种 ABC 型聚(2-乙基-2-恶唑啉)-b-聚(2-正丙基-2-恶唑啉)-b-聚(2-甲基-2-恶唑啉)三嵌段共聚物,具有热敏性中间嵌段。最后,制备了具有不同摩尔质量和两亲平衡的聚乙二醇-b-聚丁二醇-b-聚乙二醇共聚物。中性两亲性嵌段共聚物的简单结构不足以获得增强的体内基因转染。通过 HLV 给药,双或三亲性中性嵌段共聚物通过将具有低临界溶液温度的嵌段纳入载体来提高体内转染性能。共聚物的摩尔质量似乎不会以显著方式影响载体性能。

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