跳转至内容
Merck
CN
  • Charge-controlled nanoprecipitation as a modular approach to ultrasmall polymer nanocarriers: making bright and stable nanoparticles.

Charge-controlled nanoprecipitation as a modular approach to ultrasmall polymer nanocarriers: making bright and stable nanoparticles.

ACS nano (2015-04-22)
Andreas Reisch, Anne Runser, Youri Arntz, Yves Mély, Andrey S Klymchenko
摘要

Ultrasmall polymer nanoparticles are rapidly gaining importance as nanocarriers for drugs and contrast agents. Here, a straightforward modular approach to efficiently loaded and stable sub-20-nm polymer particles is developed. In order to obtain ultrasmall polymer nanoparticles, we investigated the influence of one to two charged groups per polymer chain on the size of particles obtained by nanoprecipitation. Negatively charged carboxylate and sulfonate or positively charged trimethylammonium groups were introduced into the polymers poly(d,l-lactide-co-glycolide) (PLGA), polycaprolactone (PCL), and poly(methyl methacrylate) (PMMA). According to dynamic light scattering, atomic force and electron microscopy, the presence of one to two charged groups per polymer chain can strongly reduce the size of polymer nanoparticles made by nanoprecipitation. The particle size can be further decreased to less than 15 nm by decreasing the concentration of polymer in the solvent used for nanoprecipitation. We then show that even very small nanocarriers of 15 nm size preserve the capacity to encapsulate large amounts of ionic dyes with bulky counterions at efficiencies >90%, which generates polymer nanoparticles 10-fold brighter than quantum dots of the same size. Postmodification of their surface with the PEG containing amphiphiles Tween 80 and pluronic F-127 led to particles that were stable under physiological conditions and in the presence of 10% fetal bovine serum. This modular route could become a general method for the preparation of ultrasmall polymer nanoparticles as nanocarriers of contrast agents and drugs.

材料
Product Number
品牌
产品描述

Sigma-Aldrich
Trizma ® 碱, Primary Standard and Buffer, ≥99.9% (titration), crystalline
Sigma-Aldrich
N,N-二甲基甲酰胺, anhydrous, 99.8%
Sigma-Aldrich
二氯甲烷, anhydrous, ≥99.8%, contains 40-150 ppm amylene as stabilizer
Sigma-Aldrich
乙腈, anhydrous, 99.8%
Sigma-Aldrich
Trizma ® 碱, BioPerformance Certified, meets EP, USP testing specifications, suitable for cell culture, ≥99.9% (titration)
Sigma-Aldrich
磷酸钠 一元, ReagentPlus®, ≥99.0%
Sigma-Aldrich
三(羟甲基)氨基甲烷, ACS reagent, ≥99.8%
Sigma-Aldrich
缓血酸胺, meets USP testing specifications
Sigma-Aldrich
牛磺酸, ≥99%
Sigma-Aldrich
Sigma 7-9®®, ≥99% (titration), powder or crystals
Sigma-Aldrich
甲基丙烯酸, contains 250 ppm MEHQ as inhibitor, 99%
Sigma-Aldrich
磷酸钠 一元, BioReagent, Molecular Biology, anhydrous, ≥98%
Sigma-Aldrich
Trizma ® 碱, BioUltra, Molecular Biology, ≥99.8% (T)
Sigma-Aldrich
N,N-二甲基甲酰胺, Molecular Biology, ≥99%
Sigma-Aldrich
罗丹明B, ≥95% (HPLC)
Sigma-Aldrich
磷酸钠 二元, ReagentPlus®, ≥99.0%
Sigma-Aldrich
1-羟基苯并三唑 水合物, ≥97.0% dry basis (T)
Sigma-Aldrich
罗丹明B, suitable for fluorescence
Sigma-Aldrich
磷酸钠 二元, BioReagent, suitable for cell culture, suitable for insect cell culture, ≥99.0%
Sigma-Aldrich
磷酸钠 一元, BioPerformance Certified, suitable for cell culture, suitable for insect cell culture, suitable for plant cell culture, ≥99.0% (titration)
Sigma-Aldrich
L-赖氨酸 单盐酸盐, from non-animal source, meets EP, JP, USP testing specifications, suitable for cell culture, 98.5-101.0%
Sigma-Aldrich
磷酸钠 二元, BioXtra, ≥99.0%
Sigma-Aldrich
磷酸钠 二元, Molecular Biology, ≥98.5% (titration)
Sigma-Aldrich
丁二酸酐, ≥99% (GC)
Sigma-Aldrich
牛磺酸, suitable for cell culture, meets USP testing specifications
Sigma-Aldrich
Trizma ® 碱, ≥99.0% (T)
Sigma-Aldrich
磷酸氢二钠 溶液, BioUltra, 0.5 M in H2O
Sigma-Aldrich
Trizma ® 碱, BioXtra, pH 10.5-12.0 (1 M in H2O), ≥99.9% (titration)
Sigma-Aldrich
磷酸钠 一元, meets USP testing specifications, anhydrous
Sigma-Aldrich
磷酸二氢钠 溶液, BioUltra, 5 M in H2O