Instead of veterinary school, Adler-Moore earned her doctorate in medical microbiology from Cornell University Graduate School of Medical Sciences in New York City. Though she had offers from other universities, she joined the faculty of
California State Polytechnic University, Pomona in 1974.
"CSU students were the ones I wanted to be with," she says. "These are kids with a really strong work ethic who don't expect things are just going to be handed to them. And because of the smaller class size, I'd be able to really get to know my students."
The young professor began applying for grants almost from the day she arrived. The funding allowed her to set up a lab at Cal Poly Pomona and, later, to train high school science teachers in how to introduce molecular biology techniques into their own classrooms.
By the early '80s, the field of biotechnology was starting to ignite. In 1983, Adler-Moore took a sabbatical to consult with a local biotech firm. She had an idea for a new kind of drug, one that would wipe out the often-deadly fungal infections that affect patients with a weakened immune system, such as people who are HIV-positive, transplant recipients, cancer patients, hospitalized patients, and those taking steroid medications.
The drug had to be better than amphotericin B, the only option to treat the infections. "This drug option was really toxic," she says. "It would cause people to have fever and chills and violent vomiting and their kidneys would get destroyed. But there was no alternative."
Adler-Moore knew that some toxic cancer chemotherapy drugs could be wrapped in microscopic fatty bubbles called liposomes that made the drug less harmful to patients, but still effective in fighting cancer. Could the process work the same way, she wondered, to kill fungi?