Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Ildiko Csoka"'
Autor:
Anett Motzwickler-Németh, Petra Party, Péter Simon, Milena Sorrenti, Rita Ambrus, Ildikó Csóka
Publikováno v:
Pharmaceutics, Vol 16, Iss 11, p 1361 (2024)
Background/Objectives: Research on cyclodextrin-based metal-organic frameworks (CD-MOFs) is still in its infancy, but their potential for use in drug delivery—expressly in the lung—seems promising. We aimed to use the freeze-drying method to crea
Externí odkaz:
https://doaj.org/article/caef28ccd78b4979bd282871c010e92b
Publikováno v:
Pharmaceutics, Vol 14, Iss 7, p 1329 (2022)
Solvent-free preparation types for cyclodextrin complexation, such as co-grinding, are technologies desired by the industry. However, in-depth analytical evaluation of the process and detailed characterization of intermediate states of the complexes
Externí odkaz:
https://doaj.org/article/8306eb5da431455485f2df8e61fd121b
Autor:
Gábor Katona, Fakhara Sabir, Bence Sipos, Muhammad Naveed, Zsuzsanna Schelz, István Zupkó, Ildikó Csóka
Publikováno v:
Pharmaceutics, Vol 14, Iss 3, p 631 (2022)
This work aimed to develop lomustine (LOM) and n-propyl gallate (PG)-loaded liposomes suitable for targeting glioblastoma multiforme (GBM) via the auspicious nose-to-brain drug delivery pathway. The therapeutical effect of LOM, as a nitrosourea compo
Externí odkaz:
https://doaj.org/article/1d6d960b9f6a481090a060540e69d72f
Autor:
Réka Szoleczky, Mária Budai-Szűcs, Erzsébet Csányi, Szilvia Berkó, Péter Tonka-Nagy, Ildikó Csóka, Anita Kovács
Publikováno v:
Pharmaceutics, Vol 14, Iss 4, p 707 (2022)
The aim of our study was to adapt the analytical quality by design (AQbD) approach to design an effective in vitro release test method using USP apparatus IV with a semi-solid adapter (SSA) for diclofenac sodium hydrogel. The analytical target profil
Externí odkaz:
https://doaj.org/article/7b19e0b79c434524a4147ba4c0d30030
Autor:
Balázs Attila Kondoros, Orsolya Jójárt-Laczkovich, Ottó Berkesi, Piroska Szabó-Révész, Ildikó Csóka, Rita Ambrus, Zoltán Aigner
Publikováno v:
Pharmaceutics, Vol 14, Iss 4, p 744 (2022)
Molecular complexation with cyclodextrins (CDs) has long been a known process for modifying the physicochemical properties of problematic active pharmaceutical ingredients with poor water solubility. In current times, the focus has been on the solven
Externí odkaz:
https://doaj.org/article/2f7bcc9b7af94600b98f3f771c9a8ec2
Autor:
Ernő Benkő, Ilija German Ilič, Katalin Kristó, Géza Regdon, Ildikó Csóka, Klára Pintye-Hódi, Stane Srčič, Tamás Sovány
Publikováno v:
Pharmaceutics, Vol 14, Iss 2, p 228 (2022)
There is a growing interest in implantable drug delivery systems (DDS) in pharmaceutical science. The aim of the present study is to investigate whether it is possible to customize drug release from implantable DDSs through drug–carrier interaction
Externí odkaz:
https://doaj.org/article/e5681127c09c4df19f31ea8b0e58d704
Publikováno v:
Pharmaceutics, Vol 14, Iss 2, p 245 (2022)
Nanocrystal is widely applied to improve the dissolution of poorly water-soluble drugs. We aimed to prepare meloxicam (MLX) nanocrystals using the bead mill method, followed by high-pressure homogenization (HPH). Simple drying at room temperature (RD
Externí odkaz:
https://doaj.org/article/2f1fc5ec0791480ea3097535bdb98bcb
Autor:
Anita Kovács, Stella Zsikó, Fanni Falusi, Erzsébet Csányi, Mária Budai-Szűcs, Ildikó Csóka, Szilvia Berkó
Publikováno v:
Pharmaceutics, Vol 13, Iss 12, p 2106 (2021)
In recent years, the study of dermal preparations has received increased attention. There are more and more modern approaches to evaluate transdermal formulations, which are crucial in proving the efficacy of a formulation. The aim of this study was
Externí odkaz:
https://doaj.org/article/f012556fedc1439cbced5763e49a4bfe
Publikováno v:
Pharmaceutics, Vol 13, Iss 7, p 1071 (2021)
Liposomal formulation development is a challenging process. Certain factors have a critical influence on the characteristics of the liposomes, and even the relevant properties can vary based on the predefined interests of the research. In this paper,
Externí odkaz:
https://doaj.org/article/32afa1bb39c848af9b25df6fc01e3e33
Publikováno v:
Pharmaceutics, Vol 13, Iss 5, p 702 (2021)
Nanoparticle research and development for pharmaceuticals is a challenging task in the era of personalized medicine. Specialized and increased patient expectations and requirements for proper therapy adherence, as well as sustainable environment safe
Externí odkaz:
https://doaj.org/article/9de6fef12b174e8480e4a596446737a2