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L6 肌细胞系作为评估肠胃外给药产品刺激性的工具。

The L6 muscle cell line as a tool to evaluate parenteral products for irritation.

作者信息

Laska D A, Williams P D, Reboulet J T, Morris R M

机构信息

Toxicology Division, Lilly Research Laboratories, Greenfield, IN 46140.

出版信息

J Parenter Sci Technol. 1991 Mar-Apr;45(2):77-82.

PMID:2051260
Abstract

A rat skeletal muscle cell line (L6) was evaluated for its utility in assessing cellular damage caused by parenteral administration of eight commercially available pharmaceuticals. The physical forms of the eight pharmaceuticals were diverse, including aqueous and non-aqueous suspensions and solutions. The L6 cells were exposed to therapeutic as well as diluted concentrations of methocarbamol, lorazepam, dimercaprol, phytonadione, menadiol sodium phosphate, penicillin G procaine, penicillin G benzathine, and iron dextran complex. Irritation assessment was based on the depletion of creatine phosphokinase (CK) from treated cultures versus untreated controls. The results obtained correlate well with reports of irritation and side effects noted in clinical use, and demonstrate the versatility of the model for testing suspensions and non-aqueous parenteral solutions. The L6 model is a useful tool to assist in determining the relative local irritancy of parenteral products.

摘要

对一种大鼠骨骼肌细胞系(L6)评估了其在评价八种市售药物肠胃外给药所引起的细胞损伤方面的效用。这八种药物的物理形态多样,包括水性和非水性混悬液及溶液。将L6细胞暴露于美索巴莫、劳拉西泮、二巯丙醇、维生素K1、磷酸甲萘氢醌钠、普鲁卡因青霉素G、苄星青霉素G和右旋糖酐铁复合物的治疗浓度以及稀释浓度下。刺激评估基于处理过的培养物中肌酸磷酸激酶(CK)相对于未处理对照的消耗情况。所得结果与临床使用中所记录的刺激和副作用报告高度相关,并证明了该模型在测试混悬液和非水性肠胃外溶液方面的通用性。L6模型是有助于确定肠胃外产品相对局部刺激性的有用工具。

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