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鱼精蛋白作为一种用于隐形眼镜消毒的潜在杀阿米巴剂。

Protamine as a potential amoebicidal agent for contact lens disinfection.

作者信息

Vijay Ajay Kumar, Bandara Mahesh, Zhu Hua, Willcox Mark Duncan P

机构信息

Brien Holden Vision Institute, Sydney, New South Wales, Australia.

出版信息

Optom Vis Sci. 2013 Feb;90(2):119-24. doi: 10.1097/OPX.0b013e31827cdabc.

Abstract

PURPOSE

To evaluate the amoebicidal efficacy of protamine with polyhexamethylene biguanide (PHMB) and ethylenediamine tetraacetic acid (EDTA).

METHODS

The International Organization for Standardization 14729:2001 procedure was modified to test amoebicidal activity. Acanthamoeba cells were inoculated into dilutions of protamine alone (57 to 228 μM) or in combination with PHMB/EDTA and incubated at 25°C for 6 hours. The number of survivors was determined after 7 days of incubation at 32°C on Escherichia coli-seeded agar plates. For encystment, Acanthamoeba trophozoites were incubated in protamine/PHMB/EDTA for 24 hours, and then the number of cysts was counted using a hemocytometer.

RESULTS

Protamine showed significant (p < 0.01) activity against trophozoites of both Acanthamoeba strains, which reached 2 log reductions or more for 228 μM compared with that in phosphate buffered saline. The addition of PHMB to protamine significantly (p = 0.002) improved anti-Acanthamoeba effect (0.8 logs reduction) of Acanthamoeba castellanii only. The addition of EDTA to protamine/PHMB only slightly improved efficacy (0.1 logs). Protamine at 228 μM significantly (p < 0.0001) killed the cysts of either strain by between 0.6 and 0.9 logs. Protamine/PHMB significantly increased killing (p = 0.014) of cysts of A. castellanii only. Protamine/PHMB/EDTA did not show synergy against Acanthamoeba cysts. Protamine or protamine/PHMB with or without EDTA did not cause encystment.

CONCLUSIONS

Protamine shows good activity against Acanthamoeba trophozoites and cysts and works more effectively in combination with PHMB against A. castellanii. Protamine may be a promising ingredient in contact lens-disinfecting solutions to control Acanthamoeba growth.

摘要

目的

评估鱼精蛋白与聚六亚甲基双胍(PHMB)和乙二胺四乙酸(EDTA)联合使用时的杀阿米巴原虫效果。

方法

对国际标准化组织14729:2001的程序进行修改以测试杀阿米巴原虫活性。将棘阿米巴细胞接种到单独的鱼精蛋白稀释液(57至228μM)或与PHMB/EDTA联合的稀释液中,并在25°C下孵育6小时。在接种大肠杆菌的琼脂平板上于32°C孵育7天后测定存活者数量。对于包囊形成,将棘阿米巴滋养体在鱼精蛋白/PHMB/EDTA中孵育24小时,然后使用血细胞计数器计数包囊数量。

结果

鱼精蛋白对两种棘阿米巴菌株的滋养体均显示出显著(p < 0.01)活性,与磷酸盐缓冲盐水相比,228μM的鱼精蛋白可使数量减少2个对数或更多。仅向鱼精蛋白中添加PHMB可显著(p = 0.002)提高对卡氏棘阿米巴的抗棘阿米巴效果(减少0.8个对数)。仅向鱼精蛋白/PHMB中添加EDTA对效果的改善较小(0.1个对数)。228μM的鱼精蛋白可显著(p < 0.0001)杀死两种菌株的包囊,数量减少0.6至0.9个对数。仅鱼精蛋白/PHMB可显著增加对卡氏棘阿米巴包囊的杀灭(p = 0.014)。鱼精蛋白/PHMB/EDTA对棘阿米巴包囊未显示出协同作用。有或没有EDTA的鱼精蛋白或鱼精蛋白/PHMB均未导致包囊形成。

结论

鱼精蛋白对棘阿米巴滋养体和包囊均显示出良好活性,并且与PHMB联合使用时对卡氏棘阿米巴的作用更有效。鱼精蛋白可能是隐形眼镜消毒溶液中控制棘阿米巴生长的一种有前景的成分。

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