Biopolymeric Nanogel as a Drug Delivery System for Doxorubicin—Improved Drug Stability and Enhanced Antineoplastic Activity in Skin Cancer Cells

In this study, doxorubicin was loaded in a chitosan–albumin nanogel with the aim of improving its stability and exploring the potential of the system in the treatment of skin cancer. Infrared spectroscopy and X-ray diffraction confirmed the encapsulation of the drug. Transmission electron microscopy...

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Main Authors: Lyubomira Radeva, Maya M. Zaharieva, Ivanka Spassova, Daniela Kovacheva, Ivanka Pencheva-El Tibi, Hristo Najdenski, Krassimira Yoncheva
Format: Article
Language:English
Published: MDPI AG 2024-01-01
Series:Pharmaceuticals
Subjects:
Online Access:https://www.mdpi.com/1424-8247/17/2/186
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author Lyubomira Radeva
Maya M. Zaharieva
Ivanka Spassova
Daniela Kovacheva
Ivanka Pencheva-El Tibi
Hristo Najdenski
Krassimira Yoncheva
author_facet Lyubomira Radeva
Maya M. Zaharieva
Ivanka Spassova
Daniela Kovacheva
Ivanka Pencheva-El Tibi
Hristo Najdenski
Krassimira Yoncheva
author_sort Lyubomira Radeva
collection DOAJ
description In this study, doxorubicin was loaded in a chitosan–albumin nanogel with the aim of improving its stability and exploring the potential of the system in the treatment of skin cancer. Infrared spectroscopy and X-ray diffraction confirmed the encapsulation of the drug. Transmission electron microscopy revealed the spherical shape of the nanogel particles. The drug-loaded nanogel was characterized with a small diameter of 29 nm, narrow polydispersity (0.223) and positive zeta potential (+34 mV). The exposure of encapsulated doxorubicin to light (including UV irradiation and daylight) did not provoke any degradation, whereas the nonencapsulated drug was significantly degraded. In vitro studies on keratinocytes (HaCaT) and epidermoid squamous skin carcinoma cells (A-431) disclosed that the encapsulated doxorubicin was more cytotoxic on both cell lines than the pure drug was. More importantly, the cytotoxic concentration of encapsulated doxorubicin in carcinoma cells was approximately two times lower than that in keratinocytes, indicating that it would not affect them. Thus, the loading of doxorubicin into the developed chitosan–albumin nanogel definitely stabilized the drug against photodegradation and increased its antineoplastic effect on the skin cancer cell line.
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spelling doaj.art-ff9edda0a345422fb89028d53808e0c02024-02-23T15:30:37ZengMDPI AGPharmaceuticals1424-82472024-01-0117218610.3390/ph17020186Biopolymeric Nanogel as a Drug Delivery System for Doxorubicin—Improved Drug Stability and Enhanced Antineoplastic Activity in Skin Cancer CellsLyubomira Radeva0Maya M. Zaharieva1Ivanka Spassova2Daniela Kovacheva3Ivanka Pencheva-El Tibi4Hristo Najdenski5Krassimira Yoncheva6Faculty of Pharmacy, Medical University of Sofia, 1000 Sofia, BulgariaThe Stephan Angeloff Institute of Microbiology, Bulgarian Academy of Sciences, 1113 Sofia, BulgariaInstitute of General and Inorganic Chemistry, Bulgarian Academy of Sciences, 1113 Sofia, BulgariaInstitute of General and Inorganic Chemistry, Bulgarian Academy of Sciences, 1113 Sofia, BulgariaFaculty of Pharmacy, Medical University of Sofia, 1000 Sofia, BulgariaThe Stephan Angeloff Institute of Microbiology, Bulgarian Academy of Sciences, 1113 Sofia, BulgariaFaculty of Pharmacy, Medical University of Sofia, 1000 Sofia, BulgariaIn this study, doxorubicin was loaded in a chitosan–albumin nanogel with the aim of improving its stability and exploring the potential of the system in the treatment of skin cancer. Infrared spectroscopy and X-ray diffraction confirmed the encapsulation of the drug. Transmission electron microscopy revealed the spherical shape of the nanogel particles. The drug-loaded nanogel was characterized with a small diameter of 29 nm, narrow polydispersity (0.223) and positive zeta potential (+34 mV). The exposure of encapsulated doxorubicin to light (including UV irradiation and daylight) did not provoke any degradation, whereas the nonencapsulated drug was significantly degraded. In vitro studies on keratinocytes (HaCaT) and epidermoid squamous skin carcinoma cells (A-431) disclosed that the encapsulated doxorubicin was more cytotoxic on both cell lines than the pure drug was. More importantly, the cytotoxic concentration of encapsulated doxorubicin in carcinoma cells was approximately two times lower than that in keratinocytes, indicating that it would not affect them. Thus, the loading of doxorubicin into the developed chitosan–albumin nanogel definitely stabilized the drug against photodegradation and increased its antineoplastic effect on the skin cancer cell line.https://www.mdpi.com/1424-8247/17/2/186doxorubicinnanogeldrug stabilitychitosanalbuminskin cancer
spellingShingle Lyubomira Radeva
Maya M. Zaharieva
Ivanka Spassova
Daniela Kovacheva
Ivanka Pencheva-El Tibi
Hristo Najdenski
Krassimira Yoncheva
Biopolymeric Nanogel as a Drug Delivery System for Doxorubicin—Improved Drug Stability and Enhanced Antineoplastic Activity in Skin Cancer Cells
Pharmaceuticals
doxorubicin
nanogel
drug stability
chitosan
albumin
skin cancer
title Biopolymeric Nanogel as a Drug Delivery System for Doxorubicin—Improved Drug Stability and Enhanced Antineoplastic Activity in Skin Cancer Cells
title_full Biopolymeric Nanogel as a Drug Delivery System for Doxorubicin—Improved Drug Stability and Enhanced Antineoplastic Activity in Skin Cancer Cells
title_fullStr Biopolymeric Nanogel as a Drug Delivery System for Doxorubicin—Improved Drug Stability and Enhanced Antineoplastic Activity in Skin Cancer Cells
title_full_unstemmed Biopolymeric Nanogel as a Drug Delivery System for Doxorubicin—Improved Drug Stability and Enhanced Antineoplastic Activity in Skin Cancer Cells
title_short Biopolymeric Nanogel as a Drug Delivery System for Doxorubicin—Improved Drug Stability and Enhanced Antineoplastic Activity in Skin Cancer Cells
title_sort biopolymeric nanogel as a drug delivery system for doxorubicin improved drug stability and enhanced antineoplastic activity in skin cancer cells
topic doxorubicin
nanogel
drug stability
chitosan
albumin
skin cancer
url https://www.mdpi.com/1424-8247/17/2/186
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AT ivankapenchevaeltibi biopolymericnanogelasadrugdeliverysystemfordoxorubicinimproveddrugstabilityandenhancedantineoplasticactivityinskincancercells
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AT krassimirayoncheva biopolymericnanogelasadrugdeliverysystemfordoxorubicinimproveddrugstabilityandenhancedantineoplasticactivityinskincancercells