Emerging hybrid biomaterials for oxidative stress induced photodynamic therapy

被引:6
作者
Das, Manita [1 ]
Solanki, Archana [3 ]
Ganesh, Ashwini [4 ]
Thakore, Sonal [1 ,2 ]
机构
[1] Maharaja Sayajirao Univ Baroda, Fac Sci, Dept Chem, Vadodara 3960002, India
[2] Maharaja Sayajirao Univ Baroda, Fac Sci, Inst Interdisciplinary Studies, Vadodara 3960002, India
[3] Gujarat Narmada Valley Fertilizers & Chem Ltd, Res & Dev Ctr, Bharuch 392015, India
[4] Maharaja Sayajirao Univ Baroda, Fac Pharm, Vadodara 3960002, India
关键词
Oxidative stress; Photodynamic therapy; Photosensitizers; Hybrid biomaterials; PDT mechanism; MESOPOROUS SILICA NANOPARTICLES; SINGLET OXYGEN GENERATION; GRAPHENE QUANTUM DOTS; TUMOR MICROENVIRONMENT; CELL CARCINOMA; CANCER-THERAPY; DRUG-DELIVERY; PHOTOSENSITIZERS; DENDRIMERS; EXPLORATION;
D O I
10.1016/j.pdpdt.2021.102259
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cancer therapy has undergone tremendous advancements in the past few years. The drawbacks of most of these therapies have encouraged researchers to obtain further insight into the complex chemical, biochemical and biological processes ongoing in the evolving cancer cells. These studies have led to an advent of reactive oxygen species mediated therapies to target and disrupt the cancer pathology. Photodynamic therapy (PDT) has emerged as a potent candidate for oxidative stress mediated non-invasive technique for rapid diagnosis and treatment of cancer. Towards this, biomacromolecules derived hybrid nanomaterials have contributed largely in the development of various therapeutics and theranostics for efficacious cancer management that can assist PDT. This review summarizes various hybrid biomaterials and advanced techniques that have been explored widely in the past few years for PDT application. The article also mentions some of the important in-vitro and in-vivo developments and observations explored by employing these materials for PDT application. The article also describes the interactions of these materials at the biological interface and the probable mechanism that assist in generation of oxidative stress and subsequent cell death.
引用
收藏
页数:10
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