Enhanced photodynamic therapy of TiO2/N-succinyl-chitosan composite for killing cancer cells

Authors

  • Min Ma College of Pharmacy, Shanxi Medical University, Taiyuan, Shanxi, P. R. China
  • Lu Cheng College of Pharmacy, Shanxi Medical University, Taiyuan, Shanxi, P. R. China
  • Ling Wang College of Pharmacy, Shanxi Medical University, Taiyuan, Shanxi, P. R. China; Department of Pharmacy, Linfen Fourth People’s Hospital, Linfen, Shanxi, P. R. China
  • Xing Liang College of Pharmacy, Shanxi Medical University, Taiyuan, Shanxi, P. R. China
  • LinJiao Yang College of Pharmacy, Shanxi Medical University, Taiyuan, Shanxi, P. R. China
  • AiPing Zhang College of Pharmacy, Shanxi Medical University, Taiyuan, Shanxi, P. R. China https://orcid.org/0000-0002-6367-9554

DOI:

https://doi.org/10.1590/s2175-97902022e181116

Keywords:

Photodynamic therapy, TiO2/N-succinyl-chitosan composite, Methyl thiazolyl tetrazolium assay, glioma cells (U251), Killing effect, Apoptosis

Abstract

The aim of this study was to investigate the effect of TiO2/N-succinyl-chitosan composite (TiO2/ NSCS) photodynamic therapy (PDT), while considering the effects of various light sources on the activation of photosensitizer. The methyl thiazolyl tetrazolium assay was used to examine the cell survival rate of the cells. The results showed that glioma cell strain (U251) was the most sensitive cancer cell strain to TiO2/NSCS. When the concentration of TiO2/NSCS was between 0 and 800 μg·mL-1, there was no obvious cytotoxicity to normal liver cells (HL-7702) and U251 cells. During the PDT process, the photokilling effect of TiO2/NSCS on U251 cells under ultraviolet-A (UVA) light irradiation was stronger than that of pure TiO2, and its killing effects were positively correlated with concentration and irradiation time. In addition, both UVA and visible light could excite TiO2/ NSCS, which had significant killing effect on U251 cells. The results of acridine orange/ethidium bromide fluorescent double staining and Annexin V/propidium iodide double staining indicated that TiO2/NSCS under UVA and visible light irradiation could kill U251 cells by inducing apoptosis, and the apoptosis rate of TiO2/NSCS treatment groups was higher than that of TiO2 treatment groups. Therefore, TiO2/NSCS might be used as a potential photosensitizer in PDT.

Downloads

Download data is not yet available.

References

Chen S, Cheng AC, Wang MS, Peng X. Detection of apoptosis induced by new type gosling viral enteritis virus in vitro through fluo-rescein annexin V-FITC/PI double labeling. World J Gastroenterol. 2008;14(14):2174-2178.

Cheng JJ, Li WT, Tan GH, Wang ZQ, Li SY, Jin YX. Synthesis and in vitro photodynamic therapy of chlorin derivative 131-ortho-trifluoromethyl-phenylhydrazone modified pyropheophorbide-a. Biomed Pharmacother. 2017;87:263-273.

Ding Y, Zhou L, Chen X, Wu Q, Song ZY, Wei SH, et al. Mutual sensitization mechanism and self-degradation property of drug delivery system for in vitro photodynamic therapy. Int J Pharm. 2016;498(1-2):335-346.

Feng XH, Zhang SK, Lou X. Controlling silica coating thickness on TiO2 nanoparticles for effective photodynamic therapy. Colloids Surf B. 2013;107:220-226.

Ferlay JSI, Ervik M, Dikshit R, Eser S, Mathers C, Rebelo M, et al. GLOBOCAN 2012 v1.0, Cancer Incidence and Mortality Worldwide: IARC CancerBase No. 11 [Internet]. Lyon, France: International Agency for Research on Cancer. 2013. http://globocan.iarc.fr/Default.aspx

» http://globocan.iarc.fr/Default.aspx

Feuser PE, Gaspar PC, Jacques AV, Tedesco AC, Santos Silva MCD, Ricci-Júnior E, et al. Synthesis of ZnPc loaded poly(methyl methacrylate) nanoparticles via miniemulsion polymerization for photodynamic therapy in leukemic cells. Mater Sci Eng C Mater Biol Appl. 2016;60:458-466.

Gui T, Wang Y, Mao Y, Liu J, Sun S, Cao D, et al. Comparisons of 5-aminolevulinic acid photodynamic therapy and after- loading radiotherapy in vivo in cervical cancer. Clin Transl Oncol. 2013;15(6):434-442.

Ing LY, Zin NM, Sarwar A, Katas H. Antifungal activity of chitosan nanoparticles and correlation with their physical properties. Int J Biomater. 2012,2012:632698-632707.

Kamoun EA. N-succinyl chitosan-dialdehyde starch hybrid hydrogels for biomedical applications. J Adv Res. 2016;7(1):69-77.

Kasibhatla S, Amarante-Mendes GP, Finucane D, Brunner T, Bossy-Wetzel E, Green DR. Acridine Orange/Ethidium Bromide (AO/EB) Staining to Detect Apoptosis. Csh Protoc. 2006;2006(3):4493.

Li Z, Ou-Yang Y, Liu Y, Wang YQ, Zhu XL, Zhang ZZ. Folic acid-conjugated TiO2-doped mesoporous carbonaceous nanocomposites loaded with Mitoxantrone HCl for chemo-photodynamic therapy. Photochem Photobiol Sci. 2015;14(6):1197-1206.

Li Z, Pan XB, Wang TL, Wang PN, Chen JY, Mi L. Comparison of the killing effects between nitrogen-doped and pure TiO2 on HeLa cells with visible light irradiation. Nanoscale Res Lett. 2013;8(1):96-103.

Maity B, Gadadhar S, Goswami TK, Karandeba AA, Chakravarty AR. Photo-induced anticancer activity of polypyridyl platinum(II) complexes. Eur J Med Chem. 2012;57:250-258.

Mitra AK, Agrahari V, Mandal A, Cholkar K, Natarajan C, Shah S, et al. Novel delivery approaches for cancer therapeutics. J Control Release. 2015;219(21):248-268.

Pan XB, Liang XY, Yao LF, Wang XY, Jing YY, Ma J, et al. Study of the photodynamic activity of N-Doped TiO2 nanoparticles conjugated with aluminum phthalocyanine. Nanomaterials. 2017;7(10):338-347.

Rozhkova EA, Ulasov I, Lai B, Dimitrijevic NM, Lesniak MS, Rajh T. A High-performance nanobio photocatalyst for targeted brain cancer therapy. Nano Lett. 2009;9(9):3337- 3342.

Sarin H, Kanevsky AS, Wu HT, Brimacombe KR, Fung SH, Sousa AA, et al. Effective transvascular delivery of nanoparticles across the blood-brain tumor barrier into malignant glioma cells. J Transl Med. 2008;6(1):80-95.

Schuitmaker JJ, Baas P, van Leengoed HL, van der Meulen FW, Star WM, Zandwijk NV. Photodynamic therapy: a promising new modality for the treatment of cancer. J Photoch Photobio B. 1996;34(1):3-12.

Shakeel M, Jabeen F, Shabbir S, Asghar MS, Khan MS, Chaudhry AS. Toxicity of Nano-Titanium Dioxide (TiO2- NP) Through Various Routes of Exposure: a Review. Biol Trace Elem Res. 2016;172(1):1-36.

Shang HY, Han D, Ma M, Li S, Xue WT, Zhang AP. Enhancement of the photokilling effect of TiO2 in photodynamic therapy by conjugating with reduced graphene oxide and its mechanism exploration. J Photoch Photobio B . 2017;177:112-123.

Siqueira-Moura MP, Primo FL, Espreafico EM, Tedesco AC. Development, characterization, and photocytotoxicity assessment on human melanoma of chloroaluminum phthalocyanine nanocapsules. Mater Sci Eng C Mater Biol Appl . 2013;33(3):1744-1752.

Tada DB, Suraniti E, Rossi LM, Carlos APL, Carla SO, Tathyana CT, et al. Effect of Lipid Coating on the Interaction Between Silica Nanoparticles and Membranes. J Biomed Nanotechnol. 2014;10(3):519-528.

Tada DB, Rossi LM, Leite CAP, Rosangela I, Mauricio SB. Nanoparticle Platform to Modulate Reaction Mechanism of Phenothiazine Photosensitizers. J Nanosci Nanotechnol. 2010;10(5):3100-3108.

Venkatasubbu GD, Ramasamy S, Avadhani GS, Ramakrishnan V, Kumar J. Surface modification and paclitaxel drug delivery of folic acid modified polyethylene glycol functionalized hydroxyapatite nanoparticles. Powder Technol. 2013;235(2):437-442.

Wang B, Zhang GX, Leng X, Sun ZM, Zheng SL. Characterization and improved solar light activity of vanadium doped TiO2/diatomite hybrid catalysts. J Hazard Mater. 2015;285:212-220.

Wang L, Li S, Zhang AP. Synthesis and characterization of TiO2/N-succinyl-chitosan composite. Fine Chemicals. 2016;33(3):277-282.

Wang L, Ma M, Li S, Xu YL, Zhang AP. Toxicity of N-succinyl-chitosan to bovine hemoglobin and human liver cells. Chin Pharm J. 2018;53(3):193-198.

Wang YS, Li YX, Song N. Preparation of N-succinyl- chitosans with different molecular weight and their affinity for K562 leukemia cells. Acta Polym Sin. 2004;1(3):378-382.

Xu PP, Wang RJ, Ouyang J, Chen B. A new strategy for TiO2 whiskers mediated multi-mode cancer treatment. Nanoscale Res Lett . 2015;10(1):94-105.

Yan CY, Chen DW, Gu JW, Hu HY, Zhao XL, Qiao MX. Preparation of N-Succinyl-chitosan and Their Physical-Chemical Properties as a Novel Excipient. Yakugaku Zasshi. 2006;126(9):789-793.

Yurt F, Ocakoglu K, Ince M, Colak SG, Er O, Soylu HM, et al. Photodynamic therapy and nuclear imaging activities of zinc phthalocyanine-integrated TiO2 nanoparticles in breast and cervical tumors. Chem Biol Drug Des. 2018;91(3):789-796.

Zhang AP, Sun YP. Photocatalytic killing effect of TiO2 nanoparticles on Ls-174-t human colon carcinoma cells. World J Gastroenterol . 2004;10(21):3191-3193.

Zhang HJ, Shan YF, Dong LJ. A Comparison of TiO2 and ZnO nanoparticles as photosensitizers in photodynamic therapy for cancer. J Biomed Nanotechnol . 2014;10(8):1450-1457.

Downloads

Published

2022-11-17

Issue

Section

Original Article

How to Cite

Enhanced photodynamic therapy of TiO2/N-succinyl-chitosan composite for killing cancer cells. (2022). Brazilian Journal of Pharmaceutical Sciences, 58. https://doi.org/10.1590/s2175-97902022e181116

Funding data