Kress Jeremy, Rohrbach Daniel J, Carter Kevin A, Luo Dandan, Shao Shuai, Lele Shashikant, Lovell Jonathan F, Sunar Ulas
Department of Biomedical Engineering, University at Buffalo, Buffalo, NY, USA ; Department of Biomedical, Industrial & Human Factors Engineering, Wright State University, Dayton, OH, USA.
Department of Biomedical Engineering, University at Buffalo, Buffalo, NY, USA.
Biomed Opt Express. 2015 Aug 25;6(9):3546-55. doi: 10.1364/BOE.6.003546. eCollection 2015 Sep 1.
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.
化疗的疗效在很大程度上与到达肿瘤部位的药物浓度有关。阿霉素(DOX)是一种常用的抗癌药物,其脂质体形式也被批准用于治疗卵巢癌。我们最近开发了一种卟啉-磷脂(PoP)脂质体系统,该系统能够利用近红外辐射使DOX从脂质体中按需释放,以提高DOX的生物利用度。由于其固有的荧光特性,有可能且有必要对DOX的浓度和分布进行量化,最好是无创地进行。在这里,我们使用空间频域成像对光触发药物释放在体模和动物尸体中的DOX分布进行了量化。这项研究证明了在目标区域对DOX分布进行无创定量映射的可行性。