Zobrazeno 1 - 10
of 63
pro vyhledávání: '"H. Y. Karasulu"'
Autor:
Buket Özel, Nur Selvi Günel, Irfan Akartas, H. Y. Karasulu, Ercument Karasulu, Barış Gümüştaş, Güliz Ak, Şenay Hamarat Şanlıer
The main objective of this study was to prepare cisplatin (CDDP) bound triblock polymeric micelle solution which will have a hydrophilic shell not being phagocytosed by mononuclear phagocyte system, and evaluate in vitro behavior for the treatment of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d74e30f47a455922f0ffb1da590d6076
https://aperta.ulakbim.gov.tr/record/239076
https://aperta.ulakbim.gov.tr/record/239076
Autor:
Panoraia I. Siafaka, Katerina Papadopoulou, Neslihan Üstündağ Okur, Emre Şefik Çağlar, H. Y. Karasulu, Ioannis D. Karantas, Vasilios Tsanaktsis
Publikováno v:
Pharmaceutical and Biomedical Research, Vol 5, Iss 4, Pp 27-34 (2019)
Background: Glibenclamide is a lipophilic drug widely used in type 2 diabetes treatment. However, its low bioavailability limits its use. Thus, novel formulations should be applied to improve the drug’s bioavailability. Objectives: This study aimed
2-s2.0-85078197107
Controlled drug-delivery nanotechnology is one of the most studied science fields bringing together chemists, biologists, physicists, pharmacists, and physicians to develop interdisciplinary knowledge. The main outcome followe
Controlled drug-delivery nanotechnology is one of the most studied science fields bringing together chemists, biologists, physicists, pharmacists, and physicians to develop interdisciplinary knowledge. The main outcome followe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e805094e5aa8391ce91e70db0caa6f5
https://doi.org/10.1016/b978-0-12-813932-5.00013-3
https://doi.org/10.1016/b978-0-12-813932-5.00013-3
Autor:
Ş. Güniz Küçükgüzel, Ahmet Cumaoğlu, Muhammed İhsan Han, Kemal Yelekçi, Hatice Bekci, Yeliz Yıldırım, Ercument Karasulu, Abdullahi Ibrahim Uba, Ozgur Yilmaz, H. Y. Karasulu
A new series of 1,2,4-triazole containing hydrazide-hydrazones derived from (S)-naproxen (7a-m) was synthesized in this study. The structures of these compounds were characterized by spectral (Fourier-transform infrared spectroscopy, H-1-nuclear magn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4dcf1fc32e74f4a240b1be110f3fe0bc
https://aperta.ulakbim.gov.tr/record/90637
https://aperta.ulakbim.gov.tr/record/90637
Autor:
H. Y. Karasulu, Ercument Karasulu, Uğur Önsel Türk, Sebnem Apaydin, Candeger Yilmaz, Evren Gundogdu, Tugce Turgay, I. Yildırım Şimşir
Publikováno v:
Scopus-Elsevier
Rosuvastatin calcium is commonly used statin for treatment of dyslipidemia. It has low bioavailability. The aim of this study was to develop new rosuvastatin calcium self-emulsifying drug delivery systems (SEDDS) as an alternative formulation and to
Publikováno v:
Chemical and Pharmaceutical Bulletin. 62:135-143
Naproxen (Np) is an example of a non-steroidal anti-inflammatory drug (NSAID) commonly used for the reduction of pain and inflammation. In order to develop an alternative formulation for the topical administration of Np, microemulsions were evaluated
Publikováno v:
Journal of Microencapsulation. 30:132-142
The objective of this study was to formulate imatinib (IM) loaded to water-in-oil (w/o) microemulsions as an alternative formulation for cancer therapy and to evaluate the cytotoxic effect of microemulsions Caco-2 and MCF-7. Moreover, permeability st
Publikováno v:
Drug Development Research. 70:49-56
The main objective of this study was to develop an optimal methotrexate (MTX) microemulsion (M-MTX) and to evaluate the suppressive effect of MTX-loaded microemulsion on human breast, ovarian, and prostate carcinoma cell lines. The microemulsion was
Publikováno v:
AAPS PharmSciTech. 7:E39-E45
The aim of this study was to evaluate and compare the in vitro and in vivo transdermal potential of w/o microemulsion (M) and gel (G) bases for diclofenac sodium (DS). The effect of dimethyl sulfoxide (DMSO) as a penetration enhancer was also examine
Publikováno v:
Drug Development Research. 65:17-25
In order to increase topical penetration of the nonsteroidal anti-inflammatory drug, diclofenac sodium, new microemulsion formulations were prepared to increase drug solubility and in vitro penetration of the drug. The influence of dimethyl sulfoxide