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重组甲硫氨酰人粒细胞集落刺激因子(r-huG-CSF)经气管内滴注至仓鼠后在肺部的吸收情况。

Pulmonary absorption of recombinant methionyl human granulocyte colony stimulating factor (r-huG-CSF) after intratracheal instillation to the hamster.

作者信息

Niven R W, Lott F D, Cribbs J M

机构信息

Amgen Inc., Thousand Oaks, California 91320.

出版信息

Pharm Res. 1993 Nov;10(11):1604-10. doi: 10.1023/a:1018920619424.

Abstract

Recombinant methionyl human granulocyte colony stimulating factor (G-CSF), a molecule of 18.8 kDa, has been shown to induce a systemic response after delivery by aerosol. In this work, rate and extent of absorption as well as the response were determined after bolus administration of solutions by intratracheal instillation (IT). The protein was quantified using a specific ELISA and the biological response was assessed by monitoring the increase in numbers of circulating white blood cells (WBC). A dose-response curve was obtained after IT, subcutaneous injection (SC), and intracardiac injection (IC) of 100 microL of a nominal dose ranging from 1 to 1000 micrograms/kg G-CSF (n = 5). WBC numbers were determined 24 hr postadministration. Absorption and clearance kinetics were determined after IT and IC of 500 micrograms/kg protein over a 24-hr time period (n = 5). The response of the lung to G-CSF was monitored by WBC counts and differentials in lung lavage fluid. 73.6 +/- 10.5% (n = 7) of the IT dose reached the lung lobes. The response to single doses of G-CSF by IT or SC was similar, with WBC numbers increasing over 4x baseline at the higher doses. Absorption from the lung was rapid and did not follow first-order kinetics. Clearance after the IC dose was described by a biexponential equation (alpha = 1.41, beta = 0.24 hr-1). Peak serum levels were obtained approximately 1-2 hr after IT. The bioavailability was 45.9% of the administered dose and 62.0% of the dose reaching the lung lobes. These results indicate that G-CSF is rapidly absorbed from the lung.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

重组甲硫氨酰人粒细胞集落刺激因子(G-CSF),分子量为18.8 kDa,经气溶胶给药后已显示可引发全身反应。在本研究中,通过气管内滴注(IT)给予溶液推注后,测定了吸收速率和程度以及反应情况。使用特异性酶联免疫吸附测定法(ELISA)对蛋白质进行定量,并通过监测循环白细胞(WBC)数量的增加来评估生物学反应。在IT、皮下注射(SC)和心内注射(IC)100 μL名义剂量范围为1至1000 μg/kg G-CSF(n = 5)后获得剂量反应曲线。给药后24小时测定WBC数量。在24小时时间段内对500 μg/kg蛋白质进行IT和IC给药后,测定吸收和清除动力学(n = 5)。通过肺灌洗液中的WBC计数和分类来监测肺对G-CSF的反应。73.6±10.5%(n = 7)的IT剂量到达肺叶。IT或SC单次给予G-CSF的反应相似,在较高剂量下WBC数量增加超过基线的4倍。肺吸收迅速,不遵循一级动力学。IC给药后的清除情况用双指数方程描述(α = 1.41,β = 0.24 hr-1)。IT给药后约1 - 2小时达到血清峰值水平。生物利用度为给药剂量的45.9%,到达肺叶剂量的62.0%。这些结果表明G-CSF可从肺中迅速吸收。(摘要截断于250字)

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