| Literature DB >> 35293714 |
Maria Poley1, Patricia Mora-Raimundo1, Yael Shammai1, Maya Kaduri1, Lilach Koren1, Omer Adir1,2, Jeny Shklover1, Janna Shainsky-Roitman1, Srinivas Ramishetti3, Francis Man4, Rafael T M de Rosales4,5, Assaf Zinger6,7, Dan Peer3, Irit Ben-Aharon8, Avi Schroeder1.
Abstract
Throughout the female menstrual cycle, physiological changes occur that affect the biodistribution of nanoparticles within the reproductive system. We demonstrate a 2-fold increase in nanoparticle accumulation in murine ovaries and uterus during ovulation, compared to the nonovulatory stage, following intravenous administration. This biodistribution pattern had positive or negative effects when drug-loaded nanoparticles, sized 100 nm or smaller, were used to treat different cancers. For example, treating ovarian cancer with nanomedicines during mouse ovulation resulted in higher drug accumulation in the ovaries, improving therapeutic efficacy. Conversely, treating breast cancer during ovulation, led to reduced therapeutic efficacy, due to enhanced nanoparticle accumulation in the reproductive system rather than at the tumor site. Moreover, chemotherapeutic nanoparticles administered during ovulation increased ovarian toxicity and decreased fertility compared to the free drug. The menstrual cycle should be accounted for when designing and implementing nanomedicines for females.Entities:
Keywords: breast cancer; fertility; gender medicine; gold nanoparticles; liposome; mRNA LNP; ovarian cancer
Year: 2022 PMID: 35293714 PMCID: PMC7613117 DOI: 10.1021/acsnano.1c07237
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 18.027