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壳聚糖和脱聚壳聚糖低聚物作为体内质粒递送的凝聚载体。

Chitosan and depolymerized chitosan oligomers as condensing carriers for in vivo plasmid delivery.

作者信息

MacLaughlin F C, Mumper R J, Wang J, Tagliaferri J M, Gill I, Hinchcliffe M, Rolland A P

机构信息

GeneMedicine Inc., 8301 New Trails Drive, The Woodlands, TX 77381-4248, USA.

出版信息

J Control Release. 1998 Dec 4;56(1-3):259-72. doi: 10.1016/s0168-3659(98)00097-2.

Abstract

Chitosan is a polysaccharide that demonstrates much potential as a gene delivery system. The ability of a commercially available chitosan and depolymerized chitosan oligomers to condense plasmid was determined using TEM and microtitration calorimetry, while the diameter and stability of the resultant complexes were measured using laser light scattering. Selected complexes were physically stable to challenge with both serum and salt solutions. Parameters such as chitosan molecular weight, plasmid concentration and charge ratio influenced such stability. The effect of including a pH-sensitive endosomolytic peptide on the physicochemical properties of the complex was determined. The presence of a pH-sensitive endosomolytic peptide enhanced the levels of reporter gene expression in Cos-1 cells 4-fold. A selected complex containing a lytic peptide was administered in the upper small intestine and colon of rabbits, and reporter gene expression was measured in defined intestinal tissues. Reporter gene expression was enhanced in defined intestinal tissues, although levels of expression remained low. The combination of strong complex stability and low in vivo expression levels suggest that uptake and/or decomplexation, but not endosomal release, may be the critical rate-limiting steps in the uptake process.

摘要

壳聚糖是一种作为基因递送系统具有很大潜力的多糖。使用透射电子显微镜(TEM)和微量滴定热分析法测定了市售壳聚糖和脱聚壳聚糖低聚物凝聚质粒的能力,同时使用激光散射法测量了所得复合物的直径和稳定性。选定的复合物在血清和盐溶液的挑战下具有物理稳定性。壳聚糖分子量、质粒浓度和电荷比等参数影响这种稳定性。确定了包含pH敏感溶酶体肽对复合物物理化学性质的影响。pH敏感溶酶体肽的存在使Cos-1细胞中报告基因的表达水平提高了4倍。将含有裂解肽的选定复合物施用于兔的上段小肠和结肠,并在特定的肠道组织中测量报告基因的表达。尽管表达水平仍然较低,但在特定的肠道组织中报告基因的表达有所增强。强复合物稳定性和低体内表达水平的结合表明,摄取和/或解聚,而非溶酶体释放,可能是摄取过程中的关键限速步骤。

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