Juniper publishers- Academic Journal of Polymer
Science
Authored by Zheng Ruan
Photodynamic Therapy Overcoming the Hypoxia Microenvironment in Tumor Tissues
hotodynamic therapy (PDT) has been broadly exploited
as an substitute therapeutic for cancer treatment since it was first
allowed for the treatment of bladder cancer in 1993 [1]. It depends on
the ability of photo sensitizers (PS) to transfer energy from light
irradiation to tumor-dissolved oxygen (O2) to produce cytotoxic reactive oxygen species (ROS) for killing cells [2,3]. In the presence of molecular oxygen (O2), PS photo activation results in the creation of reactive oxygen species (ROS) like singlet oxygen (O2)
and damage to tumor tissues. Compared with other traditional cancer
therapies such as chemotherapy, PDT is invasive and negligibly toxic
[4]. Since treatment occurs only where light is delivered, it avoids
systematic treatment. Moreover, PDT can cause an inflammation immune
response and enlargement of anti-tumor immune surveillance. These
primary and secondary reaction mechanisms provide great inspiration for
developing PDT for cancer treatment [5].
First of all, the high efficiency of the PDT agent
itself should be emphasized. The photo sensitizer with higher singlet
oxygen quantum yield could yield more ROS after the same irradiation
condition. Many dyes obtained from natural or synthetic sources with
high intersystem’s crossing (ISC) which have been used for singlet
oxygen reactions. The heavy atom effect has been a valuable chemical
approach to increase ISC in several molecules including BODIPY
chromophores [6]. Regarding of that, we have designed and synthesized a
kind of boron-dipyrromethene derivative with bromine substituted
(BDP-Br) which has shown excellent ability of generating reactive oxygen
species (ROS) upon irradiation for PDT. Then, a simply PE Gylated
BDP-Br (PEG-BDP) as some kind of macro photo sensitizer was prepared
which has shown superior cellular uptake ability and high efficiency of
imaging and curing to PDT therapy in vitro and in vivo [7].
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