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In vitro antiretroviral activity and in vivo toxicity of the potential topical microbicide copper phthalocyanine sulfate.
Styczynski, Ashley R; Anwar, Khandaker N; Sultana, Habiba; Ghanem, Abdelhamid; Lurain, Nell; Chua, Aishi; Ghassemi, Mahmood; Novak, Richard M.
Afiliação
  • Styczynski AR; Department of Infectious Disease, University of Illinois at Chicago, Chicago, IL, 60612, USA. Ashley.styczynski@gmail.com.
  • Anwar KN; Department of Internal Medicine, George Washington University, Washington, DC, 20037, USA. Ashley.styczynski@gmail.com.
  • Sultana H; , 755 North Ave NE #1319, Atlanta, GA, 30306, USA. Ashley.styczynski@gmail.com.
  • Ghanem A; Department of Infectious Disease, University of Illinois at Chicago, Chicago, IL, 60612, USA. kanwar@uic.edu.
  • Lurain N; Department of Infectious Disease, University of Illinois at Chicago, Chicago, IL, 60612, USA. sultanah@uic.edu.
  • Chua A; Department of Infectious Disease, University of Illinois at Chicago, Chicago, IL, 60612, USA. aghanem@uic.edu.
  • Ghassemi M; Department of Infectious Disease, Rush University, Chicago, IL, 60612, USA. Nell_Lurain@rush.edu.
  • Novak RM; Department of Infectious Disease, University of Illinois at Chicago, Chicago, IL, 60612, USA. jchua3@uic.edu.
Virol J ; 12: 132, 2015 Aug 30.
Article em En | MEDLINE | ID: mdl-26319137
ABSTRACT

BACKGROUND:

Copper has antimicrobial properties and has been studied for its activity against viruses, including HIV. Copper complexed within a phthalocyanine ring, forming copper (II) phthalocyanine sulfate (CuPcS), may have a role in microbicide development when used intravaginally.

METHODS:

CuPcS toxicity was tested against cervical epithelial cells, TZM-BL cells, peripheral blood mononuclear cells (PBMC), and cervical explant tissues using cell viability assays. In vivo toxicity was assessed following intravaginal administration of CuPcS in female BALB/C mice and measured using a standardized histology grading system on reproductive tract tissues. Efficacy studies for preventing infection with HIV in the presence of various non-toxic concentrations of CuPcS were carried out in TZM-BL, PBMC, and cervical explant cultures using HIV-1BAL and various pseudovirus subtypes. Non-linear regression was applied to the data to determine the EC50/90 and CC50/90.

RESULTS:

CuPcS demonstrated inhibition of HIV infection in PBMCs at concentrations that were non-toxic in cervical epithelial cells and PBMCs with EC50 values of approximately 50 µg/mL. Reproductive tract tissue analysis revealed no toxicity at 100 mg/mL. Human cervical explant tissues challenged with HIV in the presence of CuPcS also revealed a dose-response effect at preventing HIV infection at non-toxic concentrations with an EC50 value of 65 µg/mL.

CONCLUSION:

These results suggest that CuPcS may be useful as a topical microbicide in concentrations that can be achieved in the female genital tract.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Compostos Organometálicos / Sulfatos / Infecções por HIV / Transmissão de Doença Infecciosa / Indóis / Anti-Infecciosos Locais Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Compostos Organometálicos / Sulfatos / Infecções por HIV / Transmissão de Doença Infecciosa / Indóis / Anti-Infecciosos Locais Idioma: En Ano de publicação: 2015 Tipo de documento: Article