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戊二醛对用于制备血红蛋白类氧载体的包膜 DNA 病毒的灭活作用。

Glutaraldehyde inactivation of enveloped DNA viruses in the preparation of haemoglobin-based oxygen carriers.

机构信息

a College of Life Science , Northwest University , Xi'an , P.R. China.

b National Engineering Research Center for Miniaturized Detection System , Xi'an , P.R. China.

出版信息

Artif Cells Nanomed Biotechnol. 2018 Feb;46(1):33-38. doi: 10.1080/21691401.2017.1394875. Epub 2017 Oct 28.

DOI:10.1080/21691401.2017.1394875
PMID:29081252
Abstract

Glutaraldehyde (GA), used medically as a disinfectant and as a crosslinker for haemoglobin (Hb)-based oxygen carriers (HBOCs), was investigated for its ability to inactivate viruses during the preparation of these artificial blood substitutes. Porcine parvovirus (PPV; a non-enveloped DNA virus) and porcine pseudorabies virus (PRV; an enveloped DNA virus) were used as the virus indicators. Upon treatment with 0.1 mM GA, the titer of PRV decreased from 9.62 log to 2.62 log within 0.5 h, whereas that of PPV decreased from 7.00 log to 2.30 log in 5 h. Following treatment with 1.0 mM GA, the titer of PRV decreased from 11.00 log to 1.97 log within 0.5 h, whereas that of PPV decreased from 7.50 log to 3.43 log in 4.5 h. During the polymerization of Hb with GA, the GA concentration decreased to 1.0 and 0.1 mM within 30 and 50 min, respectively, at a GA:Hb molar ratio of 10:1, whereas at a GA:Hb molar ratio of 30:1, GA decreased to those same concentrations in 1.5 and 2.5 h, respectively. This rapid decrease in GA concentration during its polymerization with Hb indicates that GA must be added into the Hb solution in a short time in order to get as high a initial concentration as possible. In this study, the GA can only inactivate PRV effectively, given that a longer time (4.5 h) was required for it to inactivate the PPV titer. This study therefore demonstrates that GA inactivates the enveloped DNA virus only during the preparation of HBOCs.

摘要

戊二醛(GA)在医学上用作消毒剂和血红蛋白(Hb)基氧载体(HBOC)的交联剂,用于研究其在制备这些人造血液替代品时灭活病毒的能力。猪细小病毒(PPV;无包膜 DNA 病毒)和猪伪狂犬病病毒(PRV;包膜 DNA 病毒)被用作病毒指示剂。用 0.1mMGA 处理时,PRV 的滴度在 0.5 小时内从 9.62 log 下降到 2.62 log,而 PPV 的滴度在 5 小时内从 7.00 log 下降到 2.30 log。用 1.0mMGA 处理时,PRV 的滴度在 0.5 小时内从 11.00 log 下降到 1.97 log,而 PPV 的滴度在 4.5 小时内从 7.50 log 下降到 3.43 log。在 GA 与 Hb 聚合过程中,GA:Hb 摩尔比为 10:1 时,GA 浓度在 30 分钟内降至 1.0mM,50 分钟内降至 0.1mM,而 GA:Hb 摩尔比为 30:1 时,GA 浓度分别在 1.5 和 2.5 小时内降至相同浓度。GA 与 Hb 聚合过程中 GA 浓度的快速下降表明,为了获得尽可能高的初始浓度,GA 必须在短时间内加入到 Hb 溶液中。在本研究中,由于需要更长的时间(4.5 小时)才能使 PPV 滴度失活,GA 只能有效灭活 PRV。因此,本研究表明,GA 仅在 HBOCs 的制备过程中灭活包膜 DNA 病毒。

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