Li Li, Cho Hana, Yoon Kwon Hyeok, Kang Han Chang, Huh Kang Moo
Department of Polymer Science and Engineering, Chungnam National University, 99 Daehak-ro, Yuseong-gu, Daejeon 305-764, Republic of Korea.
Department of Pharmacy and Integrated Research Institute of Pharmaceutical Sciences, College of Pharmacy, The Catholic University of Korea, 43 Jibong-ro, Wonmi-gu, Bucheon-si, Gyeonggi-do 420-743, Republic of Korea.
Int J Pharm. 2014 Aug 25;471(1-2):339-48. doi: 10.1016/j.ijpharm.2014.05.064. Epub 2014 Jun 2.
Poly(ethylene glycol)-b-poly(caprolactone) (PEG-b-PCL) micelles dually loaded with both pheophorbide a (PhA) as a photosensitizer and β-carotene (CAR) as a singlet oxygen ((1)O2) scavenger were designed to control photodynamic therapy (PDT) activity in cancer treatment. The CAR in the PhA/CAR micelles significantly diminished PhA-generated (1)O2 through direct (1)O2 scavenging, whereas the CAR molecules lost their (1)O2 scavenging activity when the PhA and CAR were spatially isolated by the disintegration of the PEG-b-PCL micelles. In cell-culture systems, light irradiation at a post-treatment time that corresponded to the presence of the micelles in the blood environment induced negligible phototoxicity, whereas light irradiation at a post-treatment time that corresponded to the presence of the micelles in the intracellular environment induced remarkable phototoxicity. In addition, a longer post-treatment time induced greater internalization of PhA/CAR micelles, which resulted in higher phototoxicity, suggesting an increase in photo killing activity against the tumor cells of interest. Thus, the co-loading of a (1)O2 generator and a (1)O2 scavenger into a single micelle is a potential strategy that may be useful in facilitating more accurate and reliable PDT with site-specific controllable production of singlet oxygen species for cancer treatment.
设计了一种双负载脱镁叶绿酸a(PhA)作为光敏剂和β-胡萝卜素(CAR)作为单线态氧(¹O₂)清除剂的聚(乙二醇)-b-聚(己内酯)(PEG-b-PCL)胶束,用于控制癌症治疗中的光动力疗法(PDT)活性。PhA/CAR胶束中的CAR通过直接清除¹O₂显著减少了PhA产生的¹O₂,而当PhA和CAR通过PEG-b-PCL胶束的解体在空间上分离时,CAR分子失去了其¹O₂清除活性。在细胞培养系统中,在与血液环境中胶束存在相对应的后处理时间进行光照诱导的光毒性可忽略不计,而在与细胞内环境中胶束存在相对应的后处理时间进行光照则诱导显著的光毒性。此外,更长的后处理时间会导致PhA/CAR胶束的内化增加,从而产生更高的光毒性,这表明针对感兴趣的肿瘤细胞的光杀伤活性增加。因此,将¹O₂产生剂和¹O₂清除剂共同负载到单个胶束中是一种潜在策略,可能有助于促进更准确可靠的PDT,并在癌症治疗中实现具有位点特异性可控单线态氧物种产生的光动力疗法。