Form of presentation | Articles in international journals and collections |
Year of publication | 2018 |
Язык | английский |
|
Antipin Igor Sergeevich, author
Gubaydullin Aydar Timergalievich, author
Ermakova Alina Marselovna, author
Konovalov Aleksandr Ivanovich, author
Morozova Yuliya Ernestovna, author
Shalaeva Yana Viktorovna, author
|
|
Bazanova Olga Borisovna, author
Voloshina Aleksandra Dmitrievna, author
Zobov Vladimir Vasilevich, author
Nizameev Irek Rashatovich, author
Syakaev Viktor Vasilevich, author
|
Bibliographic description in the original language |
Ermakova A., Nanoconjugates of a calixresorcinarene derivative with methoxy poly(ethylene glycol) fragments for drug encapsulation / Ermakova A., Morozova Ju., Shalaeva Ya., Syakaev V., Gubaidullin A., Voloshina A., Zobov V., Nizameev I., Bazanova O., Antipin I., Konovalov A. // Beilstein J. Nanotechnol. – 2018. – V. 9. – P. 2057-2070. DOI:10.3762/bjnano.9.195 |
Annotation |
In order to obtain a non-toxic amphiphilic calixresorcinarene capable to form nanoconjugates for drug encapsulation, tetraundecyl-calixresorcinarene functionalized by methoxy poly(ethylene glycol) chains has been synthesized. The macrocycle obtained is characterized by low hemotoxicity. In aqueous solution it forms nanoassociates that are able to encapsulate organic substrates of different hydrophobicity, including drugs (doxorubicin, naproxen, ibuprofen, quercetin). The micelles of the macrocycle slowed down the release of the hydrophilic substrates in vitro. In physiological sodium chloride solution and phosphate-buffered saline, the micelles of the macrocycle acquire thermoresponsive properties and exhibit a temperature-controlled release of doxorubicin in vitro. The combination of the low toxicity and the encapsulation properties of the obtained calixresorcinarene–mPEG conjugate shows promising potential for the use as a supramolecular drug-delivery system. |
Keywords |
calixresorcinarene, drug encapsulation, hemotoxicity, methoxy
poly(ethylene glycol), temperature-controlled release |
The name of the journal |
BEILSTEIN JOURNAL OF NANOTECHNOLOGY
|
URL |
https://www.beilstein-journals.org/bjnano/articles/9/195 |
Please use this ID to quote from or refer to the card |
https://repository.kpfu.ru/eng/?p_id=241482&p_lang=2 |
Full metadata record |
Field DC |
Value |
Language |
dc.contributor.author |
Antipin Igor Sergeevich |
ru_RU |
dc.contributor.author |
Gubaydullin Aydar Timergalievich |
ru_RU |
dc.contributor.author |
Ermakova Alina Marselovna |
ru_RU |
dc.contributor.author |
Konovalov Aleksandr Ivanovich |
ru_RU |
dc.contributor.author |
Morozova Yuliya Ernestovna |
ru_RU |
dc.contributor.author |
Shalaeva Yana Viktorovna |
ru_RU |
dc.contributor.author |
Bazanova Olga Borisovna |
ru_RU |
dc.contributor.author |
Voloshina Aleksandra Dmitrievna |
ru_RU |
dc.contributor.author |
Zobov Vladimir Vasilevich |
ru_RU |
dc.contributor.author |
Nizameev Irek Rashatovich |
ru_RU |
dc.contributor.author |
Syakaev Viktor Vasilevich |
ru_RU |
dc.date.accessioned |
2018-01-01T00:00:00Z |
ru_RU |
dc.date.available |
2018-01-01T00:00:00Z |
ru_RU |
dc.date.issued |
2018 |
ru_RU |
dc.identifier.citation |
Ermakova A., Nanoconjugates of a calixresorcinarene derivative with methoxy poly(ethylene glycol) fragments for drug encapsulation / Ermakova A., Morozova Ju., Shalaeva Ya., Syakaev V., Gubaidullin A., Voloshina A., Zobov V., Nizameev I., Bazanova O., Antipin I., Konovalov A. // Beilstein J. Nanotechnol. – 2018. – V. 9. – P. 2057-2070. DOI:10.3762/bjnano.9.195 |
ru_RU |
dc.identifier.uri |
https://repository.kpfu.ru/eng/?p_id=241482&p_lang=2 |
ru_RU |
dc.description.abstract |
BEILSTEIN JOURNAL OF NANOTECHNOLOGY |
ru_RU |
dc.description.abstract |
In order to obtain a non-toxic amphiphilic calixresorcinarene capable to form nanoconjugates for drug encapsulation, tetraundecyl-calixresorcinarene functionalized by methoxy poly(ethylene glycol) chains has been synthesized. The macrocycle obtained is characterized by low hemotoxicity. In aqueous solution it forms nanoassociates that are able to encapsulate organic substrates of different hydrophobicity, including drugs (doxorubicin, naproxen, ibuprofen, quercetin). The micelles of the macrocycle slowed down the release of the hydrophilic substrates in vitro. In physiological sodium chloride solution and phosphate-buffered saline, the micelles of the macrocycle acquire thermoresponsive properties and exhibit a temperature-controlled release of doxorubicin in vitro. The combination of the low toxicity and the encapsulation properties of the obtained calixresorcinarene–mPEG conjugate shows promising potential for the use as a supramolecular drug-delivery system. |
ru_RU |
dc.language.iso |
ru |
ru_RU |
dc.subject |
calixresorcinarene |
ru_RU |
dc.subject |
drug encapsulation |
ru_RU |
dc.subject |
hemotoxicity |
ru_RU |
dc.subject |
methoxy
poly(ethylene glycol) |
ru_RU |
dc.subject |
temperature-controlled release |
ru_RU |
dc.title |
Nanoconjugates of a calixresorcinarene derivative with methoxy poly(ethylene glycol) fragments for drug encapsulation |
ru_RU |
dc.type |
Articles in international journals and collections |
ru_RU |
|