Dorothy L Patton

Dr. Dorothy L Patton


Research Focus & Metrics

Academic Career Length

31Years (1996-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 May 2006 in Antimicrobial Agents and Chemotherapy
Verified
Journal Article
Closed access
DPDorothy L Patton
Dorothy L Patton
YSY. T. Cosgrove Sweeney
Y. T. Cosgrove Sweeney
TMT. D. McCarthy
T. D. McCarthy
SHS. L. Hillier
S. L. Hillier
Three gel formulations (1%, 3%, and 5% [wt/wt]) of SPL7013, a dendrimer known to have antiviral (anti-human immunodeficiency virus and anti-herpes simplex virus) activities, completed a range of preclinical tests in the pigtailed macaque models for vaginally and rectally applied topical microbicide safety assessments. The vaginal safety profile of the 3% SPL7013 gel formulation was equal to that of the 1% formulation but was superior to that of the 5% formulation. The 3% SPL7013 gel was further evaluated for rectal safety and for antichlamydial efficacy with cervical challenge with Chlamydia trachomatis . This first-generation dendrimer-based product was shown to be safe to the vaginal and rectal microenvironments with repeated daily use. However, a single intravaginal application of the 3% (wt/wt) SPL7013 gel did not provide protection from the acquisition of cervical chlamydial infection.

1 May 2007 in Antimicrobial Agents and Chemotherapy
Verified
Journal Article
Closed access
DPDorothy L Patton
Dorothy L Patton
YSY. T. Cosgrove Sweeney
Y. T. Cosgrove Sweeney
JBJ. E. Balkus
J. E. Balkus
LRL. C. Rohan
L. C. Rohan
BMB. J. Moncla
B. J. Moncla
SHS. L. Hillier
S. L. Hillier
The nonnucleoside reverse transcriptase inhibitor UC781 is under development as a potential microbicide to prevent sexual transmission of human immunodeficiency virus type 1 (HIV-1). Two gel formulations of UC781 (0.1% and 1.0%) were evaluated in a range of preclinical safety assessments, including systemic absorption analysis following topical application in the pig-tailed macaque models for vaginally and rectally applied topical microbicides. High-sensitivity high-performance liquid chromatography analysis of serum samples showed that no systemic absorption of UC781 was detected after repeated vaginal or rectal application of either product. However, high levels of UC781 were detectable in the cervicovaginal lavage samples up to 6 h after product exposure. Both formulations were safe to the vaginal microenvironment, even with repeated daily use, as evidenced by colposcopy, cytokine analysis, and lack of impact on vaginal microflora. By contrast, rectal application of the 1.0% UC781 formulation caused an increased expression of numerous cytokines not observed after rectal application of the 0.1% UC781 formulation. These results provide additional support for the continued development of UC781 formulations as anti-HIV microbicides.

1 October 2002 in Sexually Transmitted Diseases
Verified
Journal Article
Closed access
DPDorothy L Patton
Dorothy L Patton
YSYvonne T. Cosgrove Sweeney
Yvonne T. Cosgrove Sweeney
LRLorna K. Rabe
Lorna K. Rabe
SHSharon L. Hillier
Sharon L. Hillier
Efforts to develop topical microbicide products have all but ignored evaluation for rectal use. The goal of this study was to assess the effects of multiple rectal applications of Conceptrol (containing 4% nonoxynol-9) on flora and mucosal tissues in the pig-tailed macaque model. Monkeys (8 per group) received daily rectal applications of Conceptrol, placebo gel, or no product, for 3 days. At each visit, a preapplication rectal lavage specimen and swab specimen for microbiology and pH determination were collected. Conceptrol or placebo gel (2.5 ml) was then administered intrarectally. Fifteen minutes after application, samples were again collected. Gross observation of rectal lavage indicated sheets of epithelium 15 minutes after application of the nonoxynol-9 product. Histopathology of these samples revealed epithelial sheets with stroma attached. The presence of H2O2-producing lactobacilli remained relatively constant, whereas that of H2O2-producing viridans streptococci diminished in all nonoxynol-9-exposed animals in which these organisms were detected at baseline. Repeated applications of nonoxynol-9 disrupts the rectal mucosa of the pig-tailed macaque. The disruption of these tissues could have serious implications for an increase in likelihood of acquisition of sexually transmitted infection/HIV in humans.

1 May 2004 in Sexually Transmitted Diseases
Verified
Journal Article
Closed access
DPDorothy L Patton
Dorothy L Patton
YSY. C. Sweeney
Y. C. Sweeney
PCP. K. Cummings
P. K. Cummings
LML. Meyn
L. Meyn
LRL. K. Rabe
L. K. Rabe
SHS. L. Hillier
S. L. Hillier
The nonhuman primate model allows for safety and efficacy testing of topical microbicide products. The goal of this study was to evaluate the safety and efficacy of vaginal and rectal applications of BufferGel (ReProtect, Inc.). The safety of repeated product applications was evaluated by microflora, pH, vaginal colposcopy, and rectal lavage. To test efficacy in preventing chlamydia, infection was documented by culture and nucleic acid amplification tests. Repeated vaginal or rectal applications of BufferGel were not associated with significant changes in microflora. BufferGel use had a transient acidifying effect on vaginal and rectal pH. Colposcopic observations remained relatively normal in all test animals. A slightly increased incidence of epithelial desquamation was noted after rectal product use compared with the control group. BufferGel did not prevent cervical or rectal chlamydial infection. BufferGel has an acceptable safety profile after repeated vaginal and rectal use, but does not prevent chlamydial infection in the macaque models.

1 July 2005 in The Journal of Infectious Diseases
Verified
Journal Article
Open access
PDF file
DPDorothy L Patton
Dorothy L Patton
YSYvonne T. Cosgrove Sweeney
Yvonne T. Cosgrove Sweeney
WSWalter E. Stamm
Walter E. Stamm
We inoculated 45 female macaques in the cervix with Chlamydia trachomatis once weekly for 5 weeks and randomly assigned them to treatment with doxycy

17 March 2004 in Journal of Medical Primatology
Verified
Journal Article
Closed access
PDF file
DPDorothy L Patton
Dorothy L Patton
YSYvonne C. Sweeney
Yvonne C. Sweeney
CTChe‐Chung Tsai
Che‐Chung Tsai
SHSharon L. Hillier
Sharon L. Hillier