| Literature DB >> 26417522 |
Jeremy Kress1, Daniel J Rohrbach1, Kevin A Carter2, Dandan Luo2, Shuai Shao2, Shashikant Lele3, Jonathan F Lovell2, Ulas Sunar1.
Abstract
The efficacy of chemotherapy is related, in large part, to the concentration of drug that reaches tumor sites. Doxorubicin (DOX) is a common anti-cancer drug that is also approved for use in liposomal form for the treatment of ovarian cancer. We recently developed a porphyrin-phospholipid (PoP)-liposome system that enables on demand release of DOX from liposomes using near infrared irradiation to improve DOX bioavailability. Owing to its intrinsic fluorescence, it is possible, and desirable, to quantify DOX concentration and distribution, preferably noninvasively. Here we quantified DOX distribution following light-triggered drug release in phantoms and an animal carcass using spatial frequency domain imaging. This study demonstrates the feasibility of non-invasive quantitative mapping of DOX distributions in target areas.Entities:
Keywords: (170.0110) Imaging systems; (170.0170) Medical optics and biotechnology; (170.3880) Medical and biological imaging; (170.6935) Tissue characterization
Year: 2015 PMID: 26417522 PMCID: PMC4574678 DOI: 10.1364/BOE.6.003546
Source DB: PubMed Journal: Biomed Opt Express ISSN: 2156-7085 Impact factor: 3.732