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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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 |
work_keys_str_mv |
AT andrewgdowski developmentofbiodegradablenanocarriersloadedwithamonoclonalantibody AT amalenduranjan developmentofbiodegradablenanocarriersloadedwithamonoclonalantibody AT aninditamukerjee developmentofbiodegradablenanocarriersloadedwithamonoclonalantibody AT jamboorvishwanatha developmentofbiodegradablenanocarriersloadedwithamonoclonalantibody |
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