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  • Evaluation of polymeric nanoparticle formulations by effective imaging and quantitation of cellular uptake for controlled delivery of doxorubicin.

Evaluation of polymeric nanoparticle formulations by effective imaging and quantitation of cellular uptake for controlled delivery of doxorubicin.

Small (Weinheim an der Bergstrasse, Germany) (2014-11-18)
Khin Yin Win, Choon Peng Teng, Enyi Ye, Michelle Low, Ming-Yong Han
ABSTRACT

Various polymeric nanoparticles have been extensively engineered for applications in controlled drug release delivery in the last decades. Currently, there is a great demand to develop a strategy to qualitatively and quantitatively evaluate these polymeric nanoparticle formulations for producing innovative delivery systems. In this work, a screening platform is developed using luminescent quantum dots as drug model and imaging label to evaluate nanoparticle formulations incorporating either hydrophilic or hydrophobic drugs and imaging agents. It is validated that there is no influence of the incorporated entities on the cellular uptake profile. The use of quantum dots enables efficient detection and precise quantitation of cellular uptake of particles which occupy 25% of the cell volume. The correlation of quantum dot- and doxorubicin-incorporated nanoparticles is useful to develop an evaluation platform for nanoparticle formulations through imaging and quantitation. This platform is also used to observe the surface properties effect of other polymers such as chitosan and poly(ethylene) glycol on the cellular interaction and uptake. Moreover, quantum dots can be used to study microparticle theranostic delivery formulations by deliberately incorporating as visible ring surrounding the microparticles for their easy identifying and tracing in diagnostic and chemotherapeutic applications.

MATERIALS
Product Number
Brand
Product Description

Supelco
Sodium hydroxide concentrate, 0.1 M NaOH in water (0.1N), Eluent concentrate for IC
Sigma-Aldrich
Sodium hydroxide, BioUltra, for luminescence, ≥98.0% (T), pellets
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Sodium hydroxide solution, BioUltra, for molecular biology, 10 M in H2O
Supelco
Sodium hydroxide solution, 49-51% in water, eluent for IC
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Doxorubicin hydrochloride, suitable for fluorescence, 98.0-102.0% (HPLC)
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Acetone, natural, ≥97%
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Acetone, ≥99%, meets FCC analytical specifications
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Acetone, suitable for HPLC, ≥99.9%
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Propidium iodide, ≥94% (HPLC)
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Acetone, analytical standard
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Glycolic acid, BioXtra, ≥98.0% (titration)
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Propidium iodide, ≥94.0% (HPLC)
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Doxorubicin hydrochloride, 98.0-102.0% (HPLC)
Doxorubicin hydrochloride, European Pharmacopoeia (EP) Reference Standard
Supelco
Acetone, Pharmaceutical Secondary Standard; Certified Reference Material
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Sodium hydroxide, BioXtra, ≥98% (acidimetric), pellets (anhydrous)
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Sodium hydroxide solution, 1.0 N, BioReagent, suitable for cell culture
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Thiazolyl Blue Tetrazolium Bromide, 98%
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Glycolic acid solution, technical grade, 70 wt. % in H2O
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Glycolic acid, ReagentPlus®, 99%
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Thiazolyl Blue Tetrazolium Bromide, powder, BioReagent, suitable for cell culture, suitable for insect cell culture, ≥97.5% (HPLC)
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3-Ethyl-2,4-pentanedione, mixture of tautomers, 98%
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Glycolic acid solution, high purity, 70 wt. % in H2O
Supelco
Glycolic acid, certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland
USP
Doxorubicin hydrochloride, United States Pharmacopeia (USP) Reference Standard
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Sodium hydroxide, anhydrous, free-flowing, Redi-Dri, reagent grade, ≥98%, pellets
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Glycolic Acid, Pharmaceutical Secondary Standard; Certified Reference Material
USP
Acetone, United States Pharmacopeia (USP) Reference Standard
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Sodium hydroxide, pellets, semiconductor grade, 99.99% trace metals basis
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Sodium hydroxide, ACS reagent, ≥97.0%, pellets