Encapsulation and release of calcein from herceptin-conjugated eLiposomes

Achieving an optimal therapeutic level is crucial in effectively eradicating cancer cells during treatment. However, conventional chemotherapy-associated systemic administration of anticancer agents leads to many side effects. To achieve the desired control over the target site, active targeting of...

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Main Authors: Mah Noor Zafar, William G. Pitt, Ghaleb A. Husseini
Format: Article
Language:English
Published: Elsevier 2024-03-01
Series:Heliyon
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2405844024039136
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author Mah Noor Zafar
William G. Pitt
Ghaleb A. Husseini
author_facet Mah Noor Zafar
William G. Pitt
Ghaleb A. Husseini
author_sort Mah Noor Zafar
collection DOAJ
description Achieving an optimal therapeutic level is crucial in effectively eradicating cancer cells during treatment. However, conventional chemotherapy-associated systemic administration of anticancer agents leads to many side effects. To achieve the desired control over the target site, active targeting of HER2-positive breast cancer cells can be achieved by conjugating liposomal vesicles with Human Epidermal growth factor Receptor 2 (HER2) and inducing release of the encapsulated drug using ultrasound. To further enhance the delivery efficiency, nanoemulsion droplets exhibiting responsiveness to low-frequency ultrasound are encapsulated within these lipid vesicles. In this study, we prepared four different liposomal formulations, namely pegylated liposomes, emulsion liposomes (eLiposomes), HER-conjugated liposomes, and HER-conjugated eLiposomes, each loaded with calcein and subjected to a thorough characterization process. Their sizes, phospholipid concentration, and amount of antibody conjugation were compared and analyzed. Cryogenic transmission electron microscopy was used to confirm the encapsulation of nanoemulsion droplets within the liposomes. The drug-releasing performance of Herceptin-conjugated eLiposomes was found to surpass that of other liposomal formulations with a notably higher calcein release and established it as a highly effective nanocarrier. The study showcases the efficacy of calcein-loaded and Herceptin-conjugated eLiposomes, which demonstrate rapid and efficient drug release among other liposomal formulations when subjected to ultrasound. This discovery paves the way for a more targeted, efficient, and humane approach to cancer therapy.
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spelling doaj.art-6d3b50d19f184099b5a16cfb51b8f52b2024-04-04T05:06:14ZengElsevierHeliyon2405-84402024-03-01106e27882Encapsulation and release of calcein from herceptin-conjugated eLiposomesMah Noor Zafar0William G. Pitt1Ghaleb A. Husseini2Biomedical Engineering Program, College of Engineering, American University of Sharjah, Sharjah, P.O. Box. 26666, United Arab EmiratesDepartment of Chemical Engineering, Brigham Young University, Provo, UT, 84602, USAMaterials Science and Engineering Ph.D. Program, College of Arts and Sciences, American University of Sharjah, Sharjah, P.O. Box. 26666, United Arab Emirates; Department of Chemical and Biological Engineering, College of Engineering, American University of Sharjah, Sharjah, P.O. Box 26666, United Arab Emirates; Corresponding author. Materials Science and Engineering Ph.D. Program, College of Arts and Sciences, American University of Sharjah, Sharjah, P.O. Box. 26666, United Arab Emirates.Achieving an optimal therapeutic level is crucial in effectively eradicating cancer cells during treatment. However, conventional chemotherapy-associated systemic administration of anticancer agents leads to many side effects. To achieve the desired control over the target site, active targeting of HER2-positive breast cancer cells can be achieved by conjugating liposomal vesicles with Human Epidermal growth factor Receptor 2 (HER2) and inducing release of the encapsulated drug using ultrasound. To further enhance the delivery efficiency, nanoemulsion droplets exhibiting responsiveness to low-frequency ultrasound are encapsulated within these lipid vesicles. In this study, we prepared four different liposomal formulations, namely pegylated liposomes, emulsion liposomes (eLiposomes), HER-conjugated liposomes, and HER-conjugated eLiposomes, each loaded with calcein and subjected to a thorough characterization process. Their sizes, phospholipid concentration, and amount of antibody conjugation were compared and analyzed. Cryogenic transmission electron microscopy was used to confirm the encapsulation of nanoemulsion droplets within the liposomes. The drug-releasing performance of Herceptin-conjugated eLiposomes was found to surpass that of other liposomal formulations with a notably higher calcein release and established it as a highly effective nanocarrier. The study showcases the efficacy of calcein-loaded and Herceptin-conjugated eLiposomes, which demonstrate rapid and efficient drug release among other liposomal formulations when subjected to ultrasound. This discovery paves the way for a more targeted, efficient, and humane approach to cancer therapy.http://www.sciencedirect.com/science/article/pii/S2405844024039136EmulsionsLiposomeseLiposomesCalceinDrug deliveryUltrasound
spellingShingle Mah Noor Zafar
William G. Pitt
Ghaleb A. Husseini
Encapsulation and release of calcein from herceptin-conjugated eLiposomes
Heliyon
Emulsions
Liposomes
eLiposomes
Calcein
Drug delivery
Ultrasound
title Encapsulation and release of calcein from herceptin-conjugated eLiposomes
title_full Encapsulation and release of calcein from herceptin-conjugated eLiposomes
title_fullStr Encapsulation and release of calcein from herceptin-conjugated eLiposomes
title_full_unstemmed Encapsulation and release of calcein from herceptin-conjugated eLiposomes
title_short Encapsulation and release of calcein from herceptin-conjugated eLiposomes
title_sort encapsulation and release of calcein from herceptin conjugated eliposomes
topic Emulsions
Liposomes
eLiposomes
Calcein
Drug delivery
Ultrasound
url http://www.sciencedirect.com/science/article/pii/S2405844024039136
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