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Antimicrobial Agents and Chemotherapy, February 2008, p. 518-525, Vol. 52, No. 2
0066-4804/08/$08.00+0     doi:10.1128/AAC.00899-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Deactivation of Human Immunodeficiency Virus Type 1 in Medium by Copper Oxide-Containing Filters{triangledown}

Gadi Borkow,1,2* Humberto H. Lara,1,{dagger} Chandice Y. Covington,3,4,{ddagger} Adeline Nyamathi,4 and Jeffrey Gabbay2

Ruth Ben-Ari Institute of Clinical Immunology, Kaplan Medical Center, Hebrew University Hadassah Medical School, Rehovot 76100, Israel,1 Cupron Inc., 3704 Chiswell Ct., Greensboro, North Carolina 27410,2 College of Nursing, University of North Dakota, Grand Forks, North Dakota 58202-9025,3 School of Nursing, University of California, Los Angeles, Los Angeles, California 900954

Received 10 July 2007/ Returned for modification 17 September 2007/ Accepted 28 November 2007

Human immunodeficiency virus type 1 (HIV-1) can be transmitted through breast-feeding and through contaminated blood donations. Copper has potent biocidal properties and has been found to inactivate HIV-1 infectivity. The objective of this study was to determine the capacity of copper-based filters to inactivate HIV-1 in culture media. Medium spiked with high titers of HIV-1 was exposed to copper oxide powder or copper oxide-impregnated fibers or passed through copper-based filters, and the infectious viral titers before and after treatment were determined. Cell-free and cell-associated HIV-1 infectivity was inhibited when exposed to copper oxide in a dose-dependent manner, without cytotoxicity at the active antiviral copper concentrations. Similar dose-dependent inhibition occurred when HIV-1 was exposed to copper-impregnated fibers. Filtration of HIV-1 through filters containing the copper powder or copper-impregnated fibers resulted in viral deactivation of all 12 wild-type or drug-resistant laboratory or clinical, macrophage-tropic and T-cell-tropic, clade A, B, or C, HIV-1 isolates tested. Viral inactivation was not strain specific. Thus, a novel means to inactivate HIV-1 in medium has been developed. This inexpensive methodology may significantly reduce HIV-1 transmission from "mother to child" and/or through blood donations if proven to be effective in breast milk or plasma and safe for use. The successful application of this technology may impact HIV-1 transmission, especially in developing countries where HIV-1 is rampant.


* Corresponding author. Present address: Cupron Inc., Hameyasdim 44, Kfar Gibton 76910, Israel. Phone: 972-546-611287. Fax: 972-8-9491254. E-mail: gadi{at}cupron.com

{triangledown} Published ahead of print on 10 December 2007.

{dagger} Present address: Facultad de Ciencias Biológicas, Universidad Autónoma de Nuevo León, San Nicolás de los Garza, Nuevo León, Mexico.

{ddagger} Present address: College of Nursing, University of North Dakota, 430 Oxford Street, Stop 9025, Grand Forks, ND 58202-9025.


Antimicrobial Agents and Chemotherapy, February 2008, p. 518-525, Vol. 52, No. 2
0066-4804/08/$08.00+0     doi:10.1128/AAC.00899-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.







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