Hyperthermia-triggered release of hypoxic cell radiosensitizers from temperature-sensitive liposomes improves radiotherapy efficacy in vitro

被引:17
|
作者
Sadeghi, Negar [1 ,2 ,3 ,4 ]
Kok, Robbert Jan [2 ]
Bos, Clemens [1 ]
Zandvliet, Maurice [5 ]
Geerts, Willie J. C. [6 ]
Storm, Gert [1 ,2 ,7 ]
Moonen, Chrit T. W. [1 ]
Lammers, Twan [3 ,4 ,7 ]
Deckers, Roel [1 ]
机构
[1] Univ Med Ctr Utrecht, Imaging Div, Utrecht, Netherlands
[2] Univ Utrecht, Utrecht Inst Pharmaceut Sci, Dept Pharmaceut, Utrecht, Netherlands
[3] Rhein Westfal TH Aachen, Univ Clin, Inst Expt Mol Imaging, Dept Nanomed & Theranost, Aachen, Germany
[4] Rhein Westfal TH Aachen, Helmholtz Inst Biomed Engn, Aachen, Germany
[5] Univ Utrecht, Fac Vet Med, Dept Clin Sci Compan Anim, Utrecht, Netherlands
[6] Univ Utrecht, Bijvoet Ctr, Biomol Imaging, Utrecht, Netherlands
[7] Univ Twente, MIRA Inst Biomed Technol & Tech Med, Dept Targeted Therapeut, Enschede, Netherlands
基金
欧洲研究理事会;
关键词
nanomedicine; hyperthermia; radiotherapy; ELECTRON-AFFINIC SENSITIZATION; THERMOSENSITIVE LIPOSOMES; ENHANCED PERMEABILITY; REDUCTION POTENTIALS; PANCREATIC-CANCER; DRUG-DELIVERY; NECK-CANCER; PHASE-III; TUMOR; DOXORUBICIN;
D O I
10.1088/1361-6528/ab0ce6
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Hypoxia is a characteristic feature of solid tumors and an important cause of resistance to radiotherapy. Hypoxic cell radiosensitizers have been shown to increase radiotherapy efficacy, but dose-limiting side effects prevent their widespread use in the clinic. We propose the encapsulation of hypoxic cell radiosensitizers in temperature-sensitive liposomes (TSL) to target the radiosensitizers specifically to tumors and to avoid unwanted accumulation in healthy tissues. The main objective of the present study is to develop and characterize TSL loaded with the radiosensitizer pimonidazole (PMZ) and to evaluate the in vitro efficacy of free PMZ and PMZ encapsulated in TSL in combination with hyperthermia and radiotherapy. PMZ was actively loaded into TSL at different drug/lipid ratios, and the physicochemical characteristics and the stability of the resulting TSL-PMZ were evaluated. PMZ release was determined at 37 degrees C and 42 degrees C in HEPES buffer saline and fetal bovine serum. The concentration-dependent radiosensitizing effect of PMZ was investigated by exposing FaDu cells to different PMZ concentrations under hypoxic conditions followed by exposure to ionizing irradiation. The efficacy of TSL-PMZ in combination with hyperthermia and radiotherapy was determined in vitro, assessing cell survival and DNA damage by means of the clonogenic assay and histone H2AX phosphorylation, respectively. All TSL-PMZ formulations showed high encapsulation efficiencies and were stable for 30 d upon storage at 4 degrees C and 20 degrees C. Fast PMZ release was observed at 42 degrees C, regardless of the drug/lipid ratio. Increasing the PMZ concentration significantly enhanced the effect of ionizing irradiation. Preheated TSL-PMZ in combination with radiotherapy caused a 14.3-fold increase in cell death as compared to radiotherapy treatment alone. In conclusion, our results indicate that TSL-PMZ in combination with hyperthermia can assist in improving the efficacy of radiotherapy under hypoxic conditions.
引用
收藏
页数:13
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