Experimental study of liposomal docetaxel analysis of docetaxel incorporation and stability

Ескіз

Дата

2017

ORCID

DOI

item.page.thesis.degree.name

item.page.thesis.degree.level

item.page.thesis.degree.discipline

item.page.thesis.degree.department

item.page.thesis.degree.grantor

item.page.thesis.degree.advisor

item.page.thesis.degree.committeeMember

Назва журналу

Номер ISSN

Назва тому

Видавець

Morion LLC

Анотація

The article presents the results of developing the composition and technology of obtaining the liposomal form of docetaxel. The effect of the phospholipid composition of the membrane, ionic strength, pH, temperature, cryoprotectant type, and other factors on the stability of liposomes and the docetaxel incorporation has been considered. Results: Reduction of toxicity of the liposomal form of docetaxel (LD50 – 137 ± 7.7 mg/kg) was found in comparison with its free form (LD50 – 101 ± 6.3 mg/kg). Preservation of nanosize particle after lyophilization has been shown. Conclusions: As a result of the studies, the optimal composition and technological scheme for obtaining liposomes containing docetaxel have been developed allowing large-scale production of docetaxel in liposomal form.

Опис

Ключові слова

liposomes, docetaxel, liposomal drugs, toxicity

Бібліографічний опис

Krasnopolsky Y. M. Experimental study of liposomal docetaxel analysis of docetaxel incorporation and stability / Y. M. Krasnopolsky, А. S. Dudnichenko // Experimental Oncology. – 2017. – Vol. 39, № 2. – P. 121-123.

item.page.endorsement

item.page.review

item.page.supplemented

item.page.referenced