STUDY ON RADIOPROTECTION EFFECT FOR HUMAN LYMPHOCYTES AND FIBROBLASTS OF RESVERATROL-ENCAPSULATED LIPOSOME | Hiệp | TNU Journal of Science and Technology

STUDY ON RADIOPROTECTION EFFECT FOR HUMAN LYMPHOCYTES AND FIBROBLASTS OF RESVERATROL-ENCAPSULATED LIPOSOME

About this article

Received: 19/02/22                Revised: 18/04/22                Published: 18/04/22

Authors

1. Nguyen Minh Hiep Email to author, Center of Radiation Technology and Biotechnology
2. Pham Ngoc Duy, Center of Radiation Technology and Biotechnology
3. Vu Ngoc Bich Dao, Center of Radiation Technology and Biotechnology
4. Tran Thanh Mai, Center of Radiation Technology and Biotechnology
5. Tran Thi Ngoc Mai, Center of Radiation Technology and Biotechnology
6. Nguyen Thi Huynh Nga, Dalat University

Abstract


This study aims to evaluate radioprotection effect of resveratrol-encapsulated liposomes (Lip-RES). Firstly, Lip-RES was prepared by a combining method of lipid-film hydration method and sonication. Penetration of Lip-RES into human lymphocytes and human fibroblasts (HF cells) was observed by fluorescene microscopy. The results demonstrated that Lip-RES was successfully prepared with a relatively spherical shape, good characteristics (mean particle size of 103.9 nm, polydispersity index of 0.211, zeta potential of -31.9 mV, encapsulation efficiency of 92.31% and payload of 8.47%), and a relatively high stability. Lip-RES was well penetrated into human lymphocytes and HF cells. Under non-irradiated condition, Lip-RES showed a negligible genotoxicity, but exhibited a significant cytotoxicity for lymphocytes and HF cells at RES concentration of more than 10 µg/mL. Under irradiated condition at a dose of 2 Gy, compared to the control, Lip-RES could decrease the percentage of cell death of 16-30% and decrease the number of foci/cell of 10-15%. This indicates the radioprotection effect of Lip-RES for human lymphocytes and fibroblasts. Moreover, at a RES concentration of 2.5 µg/mL, Lip-RES showed a best radioprotection.

Keywords


Fibroblasts; Liposome; Lymphocytes; Radioprotection; Resveratrol

References


[1] A. Maciejczyk, I. Skrzypczyńsk, and M. Janiszewska, “Lung cancer. Radiotherapy in lung cancer: Actual methods and future trends,” Rep. Pract. Oncol. Radiother., vol. 19, pp. 353-360, 2014.

[2] H. A. Carvalho and R. C. Villar, “Radiotherapy and immune response: the systemic effects of a local treatment,” Clinics (Sao Paulo), vol. 73, 2018, Art. no. e557s.

[3] J. Puskin, Health risks from exposure to low level of ionizing radiation, National Research Couyncil (US) Board on Radiation Effects Research BEIR VII, Phase I, Letter Report, 1998.

[4] F. Haubner, E. Ohmann, F. Pohl, J. Strutz, and H. G. Gassner, “Wound healing after radiation therapy: Review of the literature,” Radiat. Oncol., vol. 7, p. 162, 2012.

[5] K. B. Kalpana, N. Devipriya, and M. Srinivasan, “Investigation of the radioprotective efficacy of hesperidin against gamma-radiation induced cellular damage in cultured human peripheral blood lymphocytes,” Mutat. Res. Genet. Toxicol. Environ. Mutagen., vol. 676, pp. 54-61, 2009.

[6] L. Li, M. Story, and R. J. Legerski, “Cellular responses to ionizing radiation damage,” Int. J. Radiat. Oncol., vol. 40, pp. 1157-1162, 2001.

[7] B. Salehi, A. P. Mishra, M. Nigam et al., “Resveratrol: A double-edged sword in health benefits,” Biomedicines, vol. 6, p. 91, 2018.

[8] A. Quarta, A. Gaballo, B. Pradhan et al., “Beneficial oxidative stress-related trans-resveratrol effects in the treatment and prevention of breast cancer,” Appl. Sci., vol. 11, p. 11041, 2021.

[9] M. H. Nguyen, P. N. Duy, B. Dong, K. Hadinoto et al., “Radioprotective activity of curcumin-encapsulated liposomes against genotoxicity caused by gamma Cobalt-60 irradiation in human blood cells,” Int. J. Radiat. Biol., vol. 93, pp. 1267-1273, 2017.

[10] W. Strober, “Trypan blue exclusion test of cell viability,” Curr. Protoc. Immunol., vol. 111, pp. A3.B.1-A3.B.2, 2015.

[11] K. Rothkamm and S. Horn, “Gamma-H2AX as protein biomarker for radiation exposure,” Ann. Ist. Super. Sanita., vol. 45, pp. 265-271, 2009.

[12] S. Honary and F. Zahir, “Effect of zeta potential on the properties of NanoDrug delivery systems – a review (part 2),” Trop. J. Pharm. Res., vol. 12, pp. 265-273, 2013.

[13] E. Ducat, B. Evrard, O. Peulen, and G. Piel, “Cellular uptake of liposomes monitored by confocal microscopy and flow cytometry,” J. Drug Del. Sci. Tech., vol. 21, pp. 469-477, 2011.

[14] M. S. Robert, H. Keelung, S. F. Daniel, and P. Demetrios, “Endocytosis of liposomes and intracellular fate of encapsulated molecules: Encounter with a low pH compartment after internalization in coated vesicles,” Cell, vol. 32, pp. 1069-1079, 1983.

[15] V. Berardi, F. Ricci, M. Castelli et al., “Resveratrol exhibits a strong cytotoxic activity in cultured cells and has an antiviral action against polyomavirus: potential clinical use,” J. Exp. Clin. Cancer Res., vol. 28, p. 96, 2009.

[16] C. Moreno, S. Rogero, T. Ikeda et al., “Resveratrol and radiation biological effects,” Int. J. Nutrology., vol. 5, 2012, doi: 10.1055/s-0040-1701425.




DOI: https://doi.org/10.34238/tnu-jst.5556

Refbacks

  • There are currently no refbacks.
TNU Journal of Science and Technology
Rooms 408, 409 - Administration Building - Thai Nguyen University
Tan Thinh Ward - Thai Nguyen City
Phone: (+84) 208 3840 288 - E-mail: jst@tnu.edu.vn
Based on Open Journal Systems
©2018 All Rights Reserved