TY - JOUR
T1 - Cytotoxic activity of Crotalus molossus molossus snake venom-loaded in chitosan nanoparticles against T-47D breast carcinoma cells
AU - Jimenez-Canale, Jorge
AU - Fernández-Quiroz, Daniel
AU - Teran-Saavedra, Nayelli G.
AU - Diaz-Galvez, Kevin R.
AU - Gallegos-Tabanico, Amed
AU - Burgara-Estrella, Alexel J.
AU - Sarabia-Sainz, Hector M.
AU - Guzman-Partida, Ana M.
AU - Robles-Burgueño, Maria del Refugio
AU - Vazquez-Moreno, Luz
AU - Sarabia-Sainz, Jose A.
N1 - Publisher Copyright:
© 2022,Acta Biochimica Polonica. All Rights Reserved.
PY - 2022
Y1 - 2022
N2 - Nanomedicine has led to the development of new biocompatible and biodegradable materials able to improve the pharmaceutical effect of bioactive components, broadening the options of treatment for several diseases, including cancer. Additionally, some snake venom toxins have been reported to present cytotoxic activity in different tumor cell lines, making them an auspicious option to be used as cancer drugs. The present study aims to evaluate the cytotoxic activity of the northern blacktailed rattlesnake (Crotalus molossus molossus) venomloaded chitosan nanoparticles (Cs-Venom NPs) against the T-47D breast carcinoma cell line. To do so, we first identified the significant proteins composing the venom; afterward, hemocompatibility and cytotoxic activity against tumoral cells were evaluated. The venom was then loaded into chitosan nanoparticles through the ionotropic gelation process, obtaining particles of 415.9±21.67 nm and ζ-potential of +28.3±1.17 mV. The Cs-Venom complex delivered the venom into the breast carcinoma cells, inhibiting their viability and inducing morphological changes in the T-47D cells. These features indicate that these nanoparticles are suitable for the potential use of C. m. molossus venom toxins entrapped within polymer nanoparticles for the future development and research of cancer drugs.
AB - Nanomedicine has led to the development of new biocompatible and biodegradable materials able to improve the pharmaceutical effect of bioactive components, broadening the options of treatment for several diseases, including cancer. Additionally, some snake venom toxins have been reported to present cytotoxic activity in different tumor cell lines, making them an auspicious option to be used as cancer drugs. The present study aims to evaluate the cytotoxic activity of the northern blacktailed rattlesnake (Crotalus molossus molossus) venomloaded chitosan nanoparticles (Cs-Venom NPs) against the T-47D breast carcinoma cell line. To do so, we first identified the significant proteins composing the venom; afterward, hemocompatibility and cytotoxic activity against tumoral cells were evaluated. The venom was then loaded into chitosan nanoparticles through the ionotropic gelation process, obtaining particles of 415.9±21.67 nm and ζ-potential of +28.3±1.17 mV. The Cs-Venom complex delivered the venom into the breast carcinoma cells, inhibiting their viability and inducing morphological changes in the T-47D cells. These features indicate that these nanoparticles are suitable for the potential use of C. m. molossus venom toxins entrapped within polymer nanoparticles for the future development and research of cancer drugs.
KW - Breast cancer treatment
KW - Chitosan nanoparticles
KW - Drug delivery system
KW - Nanomedicine
KW - Rattlesnake venom
UR - http://www.scopus.com/inward/record.url?scp=85125682557&partnerID=8YFLogxK
U2 - 10.18388/abp.2020_5975
DO - 10.18388/abp.2020_5975
M3 - Artículo
C2 - 35148045
AN - SCOPUS:85125682557
SN - 0001-527X
VL - 69
SP - 233
EP - 243
JO - Acta Biochimica Polonica
JF - Acta Biochimica Polonica
IS - 1
ER -