Effect of Size and Concentration of PLGA-PEG Nanoparticles on Activation and Aggregation of Washed Human Platelets

Nanotechnology is being increasingly utilised in medicine as diagnostics and for drug delivery and targeting. The small size and high surface area of nanoparticles (NPs), desirable properties that allow them to cross biological barriers, also offer potential for interaction with other cells and bloo...

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Main Authors: Rana Bakhaidar, Joshua Green, Khaled Alfahad, Shazia Samanani, Nabeehah Moollan, Sarah O’Neill, Zebunnissa Ramtoola
Format: Article
Language:English
Published: MDPI AG 2019-10-01
Series:Pharmaceutics
Subjects:
Online Access:https://www.mdpi.com/1999-4923/11/10/514
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author Rana Bakhaidar
Joshua Green
Khaled Alfahad
Shazia Samanani
Nabeehah Moollan
Sarah O’Neill
Zebunnissa Ramtoola
author_facet Rana Bakhaidar
Joshua Green
Khaled Alfahad
Shazia Samanani
Nabeehah Moollan
Sarah O’Neill
Zebunnissa Ramtoola
author_sort Rana Bakhaidar
collection DOAJ
description Nanotechnology is being increasingly utilised in medicine as diagnostics and for drug delivery and targeting. The small size and high surface area of nanoparticles (NPs), desirable properties that allow them to cross biological barriers, also offer potential for interaction with other cells and blood constituents, presenting possible safety risks. While NPs investigated are predominantly based on the biodegradable, biocompatible, and FDA approved poly-lactide-<i>co</i>-glycolide (PLGA) polymers, pro-aggregatory and antiplatelet effects have been reported for certain NPs. The potential for toxicity of PLGA based NPs remains to be examined. The aims of this study were to determine the impact of size-selected PLGA-PEG (PLGA-polyethylene glycol) NPs on platelet activation and aggregation. PLGA-PEG NPs of three average sizes of 112, 348, and 576 nm were formulated and their effect at concentrations of 0.0&#8722;2.2 mg/mL on the activation and aggregation of washed human platelets (WP) was examined. The results of this study show, for the first time, NPs of all sizes associated with the surface of platelets, with &gt;50% binding, leading to possible internalisation. The NP-platelet interaction, however, did not lead to platelet aggregation nor inhibited aggregation of platelets induced by thrombin. The outcome of this study is promising, suggesting that these NPs could be potential carriers for targeted drug delivery to platelets.
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spelling doaj.art-f8204cc5ef4b4579ac69811bc2d84dc82022-12-22T04:20:08ZengMDPI AGPharmaceutics1999-49232019-10-01111051410.3390/pharmaceutics11100514pharmaceutics11100514Effect of Size and Concentration of PLGA-PEG Nanoparticles on Activation and Aggregation of Washed Human PlateletsRana Bakhaidar0Joshua Green1Khaled Alfahad2Shazia Samanani3Nabeehah Moollan4Sarah O’Neill5Zebunnissa Ramtoola6School of Pharmacy and Biological Sciences, Royal College of Surgeons in Ireland, 2 Dublin, IrelandSchool of Medicine, Royal College of Surgeons in Ireland, 2 Dublin, IrelandSchool of Medicine, Royal College of Surgeons in Ireland, 2 Dublin, IrelandSchool of Medicine, Royal College of Surgeons in Ireland, 2 Dublin, IrelandSchool of Medicine, Royal College of Surgeons in Ireland, 2 Dublin, IrelandSchool of Pharmacy and Biological Sciences, Royal College of Surgeons in Ireland, 2 Dublin, IrelandSchool of Pharmacy and Biological Sciences, Royal College of Surgeons in Ireland, 2 Dublin, IrelandNanotechnology is being increasingly utilised in medicine as diagnostics and for drug delivery and targeting. The small size and high surface area of nanoparticles (NPs), desirable properties that allow them to cross biological barriers, also offer potential for interaction with other cells and blood constituents, presenting possible safety risks. While NPs investigated are predominantly based on the biodegradable, biocompatible, and FDA approved poly-lactide-<i>co</i>-glycolide (PLGA) polymers, pro-aggregatory and antiplatelet effects have been reported for certain NPs. The potential for toxicity of PLGA based NPs remains to be examined. The aims of this study were to determine the impact of size-selected PLGA-PEG (PLGA-polyethylene glycol) NPs on platelet activation and aggregation. PLGA-PEG NPs of three average sizes of 112, 348, and 576 nm were formulated and their effect at concentrations of 0.0&#8722;2.2 mg/mL on the activation and aggregation of washed human platelets (WP) was examined. The results of this study show, for the first time, NPs of all sizes associated with the surface of platelets, with &gt;50% binding, leading to possible internalisation. The NP-platelet interaction, however, did not lead to platelet aggregation nor inhibited aggregation of platelets induced by thrombin. The outcome of this study is promising, suggesting that these NPs could be potential carriers for targeted drug delivery to platelets.https://www.mdpi.com/1999-4923/11/10/514plga-pegnanoparticlesplateletactivationaggregationbindinguptake
spellingShingle Rana Bakhaidar
Joshua Green
Khaled Alfahad
Shazia Samanani
Nabeehah Moollan
Sarah O’Neill
Zebunnissa Ramtoola
Effect of Size and Concentration of PLGA-PEG Nanoparticles on Activation and Aggregation of Washed Human Platelets
Pharmaceutics
plga-peg
nanoparticles
platelet
activation
aggregation
binding
uptake
title Effect of Size and Concentration of PLGA-PEG Nanoparticles on Activation and Aggregation of Washed Human Platelets
title_full Effect of Size and Concentration of PLGA-PEG Nanoparticles on Activation and Aggregation of Washed Human Platelets
title_fullStr Effect of Size and Concentration of PLGA-PEG Nanoparticles on Activation and Aggregation of Washed Human Platelets
title_full_unstemmed Effect of Size and Concentration of PLGA-PEG Nanoparticles on Activation and Aggregation of Washed Human Platelets
title_short Effect of Size and Concentration of PLGA-PEG Nanoparticles on Activation and Aggregation of Washed Human Platelets
title_sort effect of size and concentration of plga peg nanoparticles on activation and aggregation of washed human platelets
topic plga-peg
nanoparticles
platelet
activation
aggregation
binding
uptake
url https://www.mdpi.com/1999-4923/11/10/514
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