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Wyszukujesz frazę "polymeric Micelles" wg kryterium: Temat


Wyświetlanie 1-5 z 5
Tytuł:
Single and multidrug filomicelles as anticancer drug delivery system
Autorzy:
Jelonek, K.
Kasperczyk, J.
Li, S.
Kaczmarczyk, B.
Orchel, A.
Musiał-Kulik, M.
Powiązania:
https://bibliotekanauki.pl/articles/284619.pdf
Data publikacji:
2016
Wydawca:
Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Polskie Towarzystwo Biominerałów
Tematy:
drug delivery system
filomicelles
polymeric Micelles
Źródło:
Engineering of Biomaterials; 2016, 19, 138; 53
1429-7248
Pojawia się w:
Engineering of Biomaterials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Preparation of scutellarin loaded TPGS polymeric micelles and evaluation of its pharmacokinetics and pharmacodynamics effects in rats
Autorzy:
Zou, Liu
Xiong, Shujuan
Deng, Xiangping
Liu, Juan
Xiong, Runde
Wang, Zhe
Cao, Xuan
Chen, Yanming
Guo, Yu
Tang, Guotao
Powiązania:
https://bibliotekanauki.pl/articles/895637.pdf
Data publikacji:
2018-12-31
Wydawca:
Polskie Towarzystwo Farmaceutyczne
Tematy:
scutellarin
TPGS
polymeric micelles
antithrombotic drugs
Opis:
To improve the clinical effect of scutellarin by extending the action time in vivo, scutellarin loaded polymeric micelles were developed by D-alpha tocopherol polyethylene glycol 1000 succinate (Scu/TPGS). Scu/TPGS were prepared using film solvent diffusion methods and characterized on the basis of their particle size, zeta potential, and drug encapsulation efficiency. Dynamic dialysis was used to study the release behavior of the polymeric micelles in vitro. Its pharmacokinetic characteristics and antithrombotic efficacy were studied by intravenous injection in rats. The results showed that Scu/TPGS were spherical, 20.09±2.62 nm in size and a slow release in vitro. The pharmacokinetic parameter T1/2 of Scu/TPGS was 762.12±46.56 min compared with commercial injection of 59.30±10.67 min (p<0.05). At the 1 mg/kg dose, the thrombolysis effect of micellar group was stronger than that of the commercial group (p<0.05). In conclusion, TPGS polymer micelles provided a valid strategy in chemotherapy for cerebrovascular diseases with poor water solubility and poor lipid solubility drugs such as scutellarin.
Źródło:
Acta Poloniae Pharmaceutica - Drug Research; 2018, 75, 6; 1305-1312
0001-6837
2353-5288
Pojawia się w:
Acta Poloniae Pharmaceutica - Drug Research
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Stimuli responsive polymeric nanoparticles in regulated drug delivery for cancer
Autorzy:
Yadav, D.
Suri, S.
Chaudhary, A.A.
-, Hemant
Beg, M. N.
Asif, M.
Ahmad, A.
Powiązania:
https://bibliotekanauki.pl/articles/949497.pdf
Data publikacji:
2012
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
regulowane podawane leków
regulowanie temperatury
regulowanie pH
micele polimerowe
rak
regulated drug delivery
temperature and pH sensitive nanoparticles
polymeric Micelles
cancer
Opis:
Stimuli-responsive drug delivery system is a concept in which a drug is delivered at a suitable rate in response to stimuli. States of diseases may cause an alteration in some parameters of the body (e.g. in tumors) and the onset and offset of the drug delivery can be done by using this as a stimuli or a "trigger". Stimuli-responsive ("intellectual" or "sharp") resources and molecules show abrupt property changes in response to miniature changes in external stimuli such as pH, temperature etc. For regulated drug delivery, environmental stimuli such as pH and temperature, which undertake phase transition in polymer system, have been investigated. Thermally-responsive polymers can be tuned to a preferred temperature variety by copolymerization with a hydrophilic co-monomer or a hydrophobic co-monomer. Hydrophilic co-monomers increase the LCST while hydrophobic co-monomers decrease the LCST. The stimuli responsive polymer for regulated drug delivery can contain a polymer and copolymers having equilibrium of hydrophilic and hydrophobic groups. A number of these polymers have been investigated extensively and some success in drug delivery with them has been achieved, such as polymers and copolymers of N-isopropylacrylamide, PLGA, and PLA, HEMA etc. Thus this review is designed for stimuli pH and temperature responsive polymeric nanoparticles, which would be helpful to treat various cronic diseases such as cancer and others, for scientists in the field of the regulated drug delivery system.
Źródło:
Polish Journal of Chemical Technology; 2012, 14, 1; 57-64
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Polymeric micelles as a new generation of anti-oxidant carriers
Micele polimerowe – nowa generacja nośników przeciwutleniaczy
Autorzy:
Arrigo, R.
Tzankova Dintcheva, N.
Catalano, G.
Morici, E.
Cavallaro, G.
Lazzara, G.
Bruno, M.
Powiązania:
https://bibliotekanauki.pl/articles/945799.pdf
Data publikacji:
2017
Wydawca:
Sieć Badawcza Łukasiewicz - Instytut Chemii Przemysłowej
Tematy:
polymeric micelles
anti-oxidant carriers
poly(ethylene oxide)
photo-oxidative stability
micele polimerowe
nośniki przeciwutleniaczy
poli(tlenek etylenu)
stabilność fotooksydacyjna
Opis:
A promising strategy to immobilize a natural stabilizer in polymeric films is presented. Particularly, nevadensin (N, a natural basil flavonoid) molecules have been encapsulated in Pluronic F-127 micelles [F127, a triblock copolymer poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide)] and the obtained nanoparticles have been introduced in poly(ethylene glycol), PEG [otherwise known as poly(ethylene oxide), PEO]. In order to verify the effectiveness of the micelles as anti-oxidant carriers, PEG-based films have been subjected to artificial weathering. The encapsulation of anti-oxidant molecules allows the enhancement of N solubility in PEG, leading to advanced materials with enhanced photo-oxidative stability.
Przedstawiono obiecującą metodę immobilizacji naturalnych przeciwutleniaczy w materiale błon polimerowych. Cząsteczki naturalnego bazyliowego flawonoidu nevadensin (N) poddawano enkapsulacji w micelach tworzących się w roztworze triblokowego kopolimeru poli(tlenek etylenu)-poli(tlenek propylenu)-poli(tlenek etylenu), [PEO-PPO-PEO] – Pluronic F-127 (F127), a otrzymane nanocząstki wprowadzano do matrycy poli(tlenku etylenu) [PEO = PEG, poli(glikolu etylenowego)]. W celu zweryfikowania efektywności miceli jako nośników przeciwutleniaczy, błony wytworzone na bazie PEG poddano procesowi sztucznego starzenia. Stwierdzono, że enkapsulacja cząstek N w micelach F127 zwiększa rozpuszczalność nevadensinu w PEG, co umożliwia otrzymanie nowatorskiego materiału o zwiększonej stabilności fotooksydacyjnej.
Źródło:
Polimery; 2017, 62, 7-8; 525-531
0032-2725
Pojawia się w:
Polimery
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Nowe rozwiązania i modyfikacje najpopularniejszych polimerowych nośników substancji aktywnych
New solutions and modifications of the most popular polymeric carriers of active substances
Autorzy:
Odrobińska, Justyna
Neugebauer, Dorota
Powiązania:
https://bibliotekanauki.pl/articles/171574.pdf
Data publikacji:
2019
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
koniugaty
micele
liposomy
nanocząstki
nośniki polimerowe
conjugates
micelles
liposomes
nanoparticles
polymeric carriers
Opis:
The progress of medicine and cosmetology corresponds to the increase in the need for new drug design and delivery methods, due to the already common cancer risk, as well as other diseases, which are still difficult for curing. Regardless of the type of active substance and its final application, the selection and synthesis of the appropriate carrier is crucial to provide the pharmaceutics to the target with the controlled release for a set period of time, including the intelligent activity. Depending on the way the bioactive substance is bound to carriers in the drug delivery systems (DDS) they are classified onto: carriers that physically encapsulate them inside i.e. liposomes, solid lipid nanoparticles, nanostructural lipid carriers, nanoparticles (nanocapsules, nanospheres), micelles, and carriers that chemically bind the active substance, i.e. conjugates, polyplexes. The current studies are emphasized to achieve the most perfect improvement, which concerns the efficiency of encapsulation, the ability to deliver several compounds simultaneously or sequentially, the productive release, the elimination of side products, the replacement of synthetic polymers by natural, biodegradable, biocompatible and non-toxic polymers. These carriers are also developed in terms of sensitivity to stimuli (one or several simultaneously or sequentially activated) and adapted for combined therapy. Although the subject of active substance delivery with the use of carriers is already widely studied, these are still a needs for the designing of new or the enhancement of the already known DDS. Working on this issue there is hope that today still incurable diseases, neoplastic diseases, as well as the diagnosis of these diseases themselves, will be possible to control and treat in the future. This report presents the current state of the knowledge in the area of DDS, focusing on newly developed solutions in the last years.
Źródło:
Wiadomości Chemiczne; 2019, 73, 9-10; 481-501
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-5 z 5

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