Open Access
Aggregation behavior of self-assembling polylactide/poly(ethylene glycol) micelles for sustained drug delivery.
Publication type: Journal Article
Publication date: 2010-07-01
scimago Q1
wos Q1
SJR: 0.988
CiteScore: 10.1
Impact factor: 5.2
ISSN: 03785173, 18733476
PubMed ID:
20434530
Pharmaceutical Science
Abstract
A series of diblock copolymers were synthesized by ring-opening polymerization of l- or d-lactide in the presence of monomethoxy poly(ethylene glycol) (mPEG) with molar masses of 2000 and 5000. The aggregation behavior of the resulting water soluble PLA/PEG diblock copolymers in aqueous medium was studied with dynamic and static light scattering (DLS and SLS), in combination with aqueous gel permeation chromatography (GPC). The average hydrodynamic radius (R(h)) of l-PLA/PEG and d-PLA/PEG mixed micelles is lower than that of l-PLA/PEG single micelles due to the stereocomplexation effect between l-PLA and d-PLA blocks. It is also confirmed that the micelle size increases with increasing temperature and hydrophobic block length, but decreases after salt addition. Aqueous GPC and SLS were used to evaluate the molecular weight (M(w)) and aggregation number (N(agg)) of the micelles. Mixed micelles present lower N(agg) than single copolymer micelles due to stereocomplexation. N(agg) decreases with increasing hydrophobic block length, and decreases upon addition of NaCl, in agreement with a more compact structure. In contrast, N(agg) increases with elevating temperature. The average radius of gyration (R(g)) and R(g)/R(h) ratio data show that both increase with increasing temperature, suggesting that micelles exhibit a compact hard-sphere structure at 15 degrees C and a swollen structure at 35 degrees C. As the temperature increases from 15 degrees C to 35 degrees C, the second virial coefficient (A(2)) of PLA/PEG copolymers turns from negative to positive, which means that water changes from poor solvent to good solvent. The fact that the average density (rho) of PLA/PEG micelles decreases with increasing temperature confirms that micelles exhibit a looser structure at higher temperatures due to water swelling effect. The higher rho value of mixed micelles as compared to single micelles also confirms a more compact structure of the former. In addition, due to the much higher N(agg) and lower R(h), PLA/PEG2000 micelles present higher rho value than PLA/PEG5000 ones.
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GOST
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Liu Y. et al. Aggregation behavior of self-assembling polylactide/poly(ethylene glycol) micelles for sustained drug delivery. // International Journal of Pharmaceutics. 2010. Vol. 394. No. 1-2. pp. 43-49.
GOST all authors (up to 50)
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Liu Y., Qi X., Liu P., El Ghzaoui A., Li S. Aggregation behavior of self-assembling polylactide/poly(ethylene glycol) micelles for sustained drug delivery. // International Journal of Pharmaceutics. 2010. Vol. 394. No. 1-2. pp. 43-49.
Cite this
RIS
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TY - JOUR
DO - 10.1016/j.ijpharm.2010.04.030
UR - https://doi.org/10.1016/j.ijpharm.2010.04.030
TI - Aggregation behavior of self-assembling polylactide/poly(ethylene glycol) micelles for sustained drug delivery.
T2 - International Journal of Pharmaceutics
AU - Liu, Yang
AU - Qi, Xu
AU - Liu, Pei
AU - El Ghzaoui, Abdelslam
AU - Li, Suming
PY - 2010
DA - 2010/07/01
PB - Elsevier
SP - 43-49
IS - 1-2
VL - 394
PMID - 20434530
SN - 0378-5173
SN - 1873-3476
ER -
Cite this
BibTex (up to 50 authors)
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@article{2010_Liu,
author = {Yang Liu and Xu Qi and Pei Liu and Abdelslam El Ghzaoui and Suming Li},
title = {Aggregation behavior of self-assembling polylactide/poly(ethylene glycol) micelles for sustained drug delivery.},
journal = {International Journal of Pharmaceutics},
year = {2010},
volume = {394},
publisher = {Elsevier},
month = {jul},
url = {https://doi.org/10.1016/j.ijpharm.2010.04.030},
number = {1-2},
pages = {43--49},
doi = {10.1016/j.ijpharm.2010.04.030}
}
Cite this
MLA
Copy
Liu, Yang, et al. “Aggregation behavior of self-assembling polylactide/poly(ethylene glycol) micelles for sustained drug delivery..” International Journal of Pharmaceutics, vol. 394, no. 1-2, Jul. 2010, pp. 43-49. https://doi.org/10.1016/j.ijpharm.2010.04.030.