注射药物溶液中乙型肝炎病毒抗原和HBV-DNA含量的稳定性。

R. Matsushita, Mariko Asahi, F. Ichimura, T. Hashimoto, E. Matsushita, S. Kaneko, Kenichi Kobayashi
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引用次数: 0

摘要

被HBV污染的注射药物溶液。然而,除了流行病学分析外,仍然没有实验证据表明乙型肝炎病毒血液交叉污染感染。此外,注射药物溶液中HBV抗原和HBV- dna含量的稳定性尚未得到分析。因此,本研究在4•Ž条件下,研究HBe阳性患者血清稀释后7天注射药物溶液(生理盐水、肝素、1%利多卡因、生理盐水中1%肝素)中HBV抗原和HBV- dna的稳定性。HBe抗原和HBV-DNA含量在7天内无明显下降。虽然HBe抗原或HBV- dna与感染能力之间的关系尚未阐明,但从HBV携带者身上抽血显然需要非常小心。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Stability of Hepatitis B Virus Antigen and HBV-DNA Contents in Injectable Drug Solutions.
jectable drug solutions with the contamination of HBV. However, there is still no experimental evidence of an infection by HBV blood cross contamination, except for epidemiological analyses. Moreover, the stability of HBV antigen and HBV-DNA contents in injectable drug solutions has not yet been analyzed. Therefore, the stability of HBV antigen and HBV-DNA in injectable drug solution (saline, heparin, 1% lidocaine, 1% heparin in saline) for 7 days under 4•Ž after dilution of HBe positive patients serum with each solution was investigated in this study. The HBe antigen and HBV-DNA contents showed no decrease for 7 days. Although the relationship between HBe antigen or HBV-DNA and infection ability, has yet to be elucidated, that drawing blood from an HBV carrier clearly requires extreme care.
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