Insertable gel for women could deliver HIV drug
Researchers have developed a vaginal suppository that, loaded with the antiviral drug Tenofovir, could help prevent the transmission of HIV and AIDS.
The semi-soft suppository is made from the seaweed-derived food ingredient carrageenan. Women could use this method to protect against the spread of sexually transmitted infections during unprotected heterosexual intercourse, the researchers say.
With more than 34 million people worldwide living with HIV, microbicides—compounds that can be applied vaginally or rectally—offer a way to slow the spread of the virus, notes lead researcher Toral Zaveri, postdoctoral scholar in the food science department at Penn State.
Containing agents known to prevent transmission of HIV and other viruses, microbicides can be inserted into the vagina prior to intercourse as a gel, cream, foam, sponge, suppository, or film.
Zaveri pointed out that carrageenan was selected over gelatin (the traditional choice for semi-soft suppositories) because it offers a number of important advantages.
Because carrageenan is plant-based, it is acceptable to vegetarians, there is no risk of animal-acquired infections, and it avoids religious objections. Also, it is more stable than gelatin at higher ambient temperatures common in tropical regions of the world.
The suppositories hold particular promise for places such as regions of Africa where HIV is widespread and women often are not in control of sexual situations, according to Zaveri.
“Condoms have been successful in preventing transmission of HIV and other sexually transmitted infections. However, effectiveness depends on correct and consistent use by the male partner,” she says.
“Due to socioeconomic and gender inequities, women in some countries and cultures are not always in a position to negotiate regular condom use, so a drug-dispersing suppository can protect against transmission of HIV and other sexually transmitted infections during heterosexual intercourse with a partner whose infection status may or may not be known to the woman.”
Testing the options
As part of the research, Zaveri, who earned her doctorate in biomedical engineering at the University of Florida, conducted extensive sensory-perception testing to assess acceptability of the suppositories among women.
Women participating in the study at the Sensory Evaluation Center in Penn State’s Department of Food Science were presented with suppositories—without the drug—in a variety of sizes, shapes, and textures.
They indicated their preferences and rated the suppositories for willingness to try and imagined ease of insertion.
The initial evaluations all were done only in the hand as part of this preclinical development effort. Many factors go into making choices, Zaveri explains, such as vaginal products women may have used previously, as well as their sexual and cultural practices.
Understanding women’s perception of the suppository and reasons behind their choices is a critical step in the development of the suppository as a vaginal drug-delivery system.
Zaveri also studied the release of Tenofovir from the suppositories in a simulated vaginal environment to ensure that the drug will be released once inserted in the body, even in the presence of semen.
“Many people work on drug delivery and use different methods to create drug-delivery products, but not many focus on the end-user aspect of this,” she says.
“Obviously, the product can be effective only if it is acceptable to women and they use it. We have gone a step farther with this study to validate the acceptability of our suppositories among women—and that’s critical.”
Why a food additive?
Zaveri notes that some may be surprised that biomedical research is done in the food science department. But she says it seemed natural given her collaboration on the study with Gregory Ziegler, who has expertise in biopolymers such as carrageenan, and John Hayes, who is known for his proficiency in sensory-perception research.
“The biomedical use of a food additive—a material widely used in the food industry for its gelling, thickening, and stabilizing properties—as a medium for a drug-delivery system is a novel idea, but we were playing to all of our strengths on the team,” she says.
Previous microbicides were generally solids or liquids.
“We exploited the intermediate design space of viscoelastic materials known as gels,” says Ziegler, “thus avoiding some of the drawbacks of these other dosage forms.”
The real beauty of the concept, Zaveri suggests, is its potential for relatively quick commercialization because the material used to formulate the suppositories, carrageenan, is already approved, and safety studies have been done in previous microbicide clinical trials.
“Currently the suppositories are prepared in the lab by simple molding,” she says. “However, the research team is investigating methods for large-scale production and packaging—key factors to be considered for product commercialization. Considering the safety, efficacy, and user-acceptability tests that we are doing, it easily is possible for a company to take this product and run with it.”
A National Institutes of Health grant to Hayes and Ziegler through the National Institute of Allergy and Infectious Diseases supported this work, which appears in PLOS ONE, Antiviral Research, and, most recently, the July and September issues of Pharmaceutics.
Source: Penn State
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