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脂质体剂量对循环中消除小单层鞘磷脂/胆固醇囊泡的影响。

Effect of liposome dose on the elimination of small unilamellar sphingomyelin/cholesterol vesicles from the circulation.

作者信息

Beaumier P L, Hwang K J, Slattery J T

出版信息

Res Commun Chem Pathol Pharmacol. 1983 Feb;39(2):277-89.

PMID:6844745
Abstract

The effect of the liposome dose of bovine brain sphingomyelin/cholesterol (2/1; mol/mol) small unilamellar vesicles (mean diameter 187 42A) on the rate of elimination of the vesicles from the circulation of mice was investigated. The results of the study indicated that the relative rate of elimination of the vesicles from the blood depended on the amount of intravenously administered liposomal lipid. The distribution of the liposomes in vivo was followed by monitoring entrapped In-111. In all tissues examined, the uptake of the liposomes was a dose-dependent process. An examination of the dose dependency of the distribution of the administered liposomes in the blood and liver at 23 hours post-injection, and of the kinetics of the elimination of these vesicles from the blood, suggests a hepatic uptake process involving two parallel pathways. One pathway is apparently a capacity-limited Michaelis-Menten process; the other pathway is a linear, non-saturable process. These pathways operate in parallel but respectively dominate at the low end and the high end of the dose range examined.

摘要

研究了牛脑鞘磷脂/胆固醇(2/1;摩尔/摩尔)小单层囊泡(平均直径187±42埃)的脂质体剂量对小鼠循环中囊泡清除率的影响。研究结果表明,囊泡从血液中的相对清除率取决于静脉注射脂质体脂质的量。通过监测包封的铟-111来追踪脂质体在体内的分布。在所有检测的组织中,脂质体的摄取是一个剂量依赖性过程。对注射后23小时给药脂质体在血液和肝脏中的分布的剂量依赖性以及这些囊泡从血液中清除的动力学进行检查,表明肝脏摄取过程涉及两条平行途径。一条途径显然是容量受限的米氏过程;另一条途径是线性的、非饱和过程。这些途径并行运作,但分别在所检测剂量范围的低端和高端占主导地位。

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