Development of Biodegradable Nanocarriers Loaded with a Monoclonal Antibody

Treatments utilizing monoclonal antibody therapeutics against intracellular protein-protein interactions in cancer cells have been hampered by several factors, including poor intracellular uptake and rapid lysosomal degradation. Our current work examines the feasibility of encapsulating monoclonal a...

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Main Authors: Andrew Gdowski, Amalendu Ranjan, Anindita Mukerjee, Jamboor Vishwanatha
Format: Article
Language:English
Published: MDPI AG 2015-02-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:http://www.mdpi.com/1422-0067/16/2/3990
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spelling doaj-66a394bed0324485b4ea7d8a5a1702122020-11-25T01:29:48ZengMDPI AGInternational Journal of Molecular Sciences1422-00672015-02-011623990399510.3390/ijms16023990ijms16023990Development of Biodegradable Nanocarriers Loaded with a Monoclonal AntibodyAndrew Gdowski0Amalendu Ranjan1Anindita Mukerjee2Jamboor Vishwanatha3Department of Molecular and Medical Genetics, University of North Texas Health Science Center, 3500 Camp Bowie Blvd, Fort Worth, TX 76107, USADepartment of Molecular and Medical Genetics, University of North Texas Health Science Center, 3500 Camp Bowie Blvd, Fort Worth, TX 76107, USADepartment of Molecular and Medical Genetics, University of North Texas Health Science Center, 3500 Camp Bowie Blvd, Fort Worth, TX 76107, USADepartment of Molecular and Medical Genetics, University of North Texas Health Science Center, 3500 Camp Bowie Blvd, Fort Worth, TX 76107, USATreatments utilizing monoclonal antibody therapeutics against intracellular protein-protein interactions in cancer cells have been hampered by several factors, including poor intracellular uptake and rapid lysosomal degradation. Our current work examines the feasibility of encapsulating monoclonal antibodies within poly(lactic-co-glycolic acid) (PLGA) nanoparticles using a water/oil/water double emulsion solvent evaporation technique. This method can be used to prepare protective polymeric nanoparticles for transporting functional antibodies to the cytoplasmic compartment of cancer cells. Nanoparticles were formulated and then characterized using a number of physical and biological parameters. The average nanoparticle size ranged from 221 to 252 nm with a low polydispersity index. Encapsulation efficiency of 16%–22% and antibody loading of 0.3%–1.12% were observed. The antibody molecules were released from the nanoparticles in a sustained manner and upon release maintained functionality. Our studies achieved successful formulation of antibody loaded polymeric nanoparticles, thus indicating that a PLGA-based antibody nanoformulation is a promising intracellular delivery vehicle for a large number of new intracellular antibody targets in cancer cells.http://www.mdpi.com/1422-0067/16/2/3990antibodynanoparticlecancerPLGAtherapyformulation
collection DOAJ
language English
format Article
sources DOAJ
author Andrew Gdowski
Amalendu Ranjan
Anindita Mukerjee
Jamboor Vishwanatha
spellingShingle Andrew Gdowski
Amalendu Ranjan
Anindita Mukerjee
Jamboor Vishwanatha
Development of Biodegradable Nanocarriers Loaded with a Monoclonal Antibody
International Journal of Molecular Sciences
antibody
nanoparticle
cancer
PLGA
therapy
formulation
author_facet Andrew Gdowski
Amalendu Ranjan
Anindita Mukerjee
Jamboor Vishwanatha
author_sort Andrew Gdowski
title Development of Biodegradable Nanocarriers Loaded with a Monoclonal Antibody
title_short Development of Biodegradable Nanocarriers Loaded with a Monoclonal Antibody
title_full Development of Biodegradable Nanocarriers Loaded with a Monoclonal Antibody
title_fullStr Development of Biodegradable Nanocarriers Loaded with a Monoclonal Antibody
title_full_unstemmed Development of Biodegradable Nanocarriers Loaded with a Monoclonal Antibody
title_sort development of biodegradable nanocarriers loaded with a monoclonal antibody
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1422-0067
publishDate 2015-02-01
description Treatments utilizing monoclonal antibody therapeutics against intracellular protein-protein interactions in cancer cells have been hampered by several factors, including poor intracellular uptake and rapid lysosomal degradation. Our current work examines the feasibility of encapsulating monoclonal antibodies within poly(lactic-co-glycolic acid) (PLGA) nanoparticles using a water/oil/water double emulsion solvent evaporation technique. This method can be used to prepare protective polymeric nanoparticles for transporting functional antibodies to the cytoplasmic compartment of cancer cells. Nanoparticles were formulated and then characterized using a number of physical and biological parameters. The average nanoparticle size ranged from 221 to 252 nm with a low polydispersity index. Encapsulation efficiency of 16%–22% and antibody loading of 0.3%–1.12% were observed. The antibody molecules were released from the nanoparticles in a sustained manner and upon release maintained functionality. Our studies achieved successful formulation of antibody loaded polymeric nanoparticles, thus indicating that a PLGA-based antibody nanoformulation is a promising intracellular delivery vehicle for a large number of new intracellular antibody targets in cancer cells.
topic antibody
nanoparticle
cancer
PLGA
therapy
formulation
url http://www.mdpi.com/1422-0067/16/2/3990
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AT aninditamukerjee developmentofbiodegradablenanocarriersloadedwithamonoclonalantibody
AT jamboorvishwanatha developmentofbiodegradablenanocarriersloadedwithamonoclonalantibody
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