Zobrazeno 1 - 10
of 13 697
pro vyhledávání: '"β−cyclodextrin"'
Autor:
Akhtar Saira, Barkat Kashif, Shahid Nariman, Anjum Irfan, Badshah Syed Faisal, Shabbir Maryam, Ibenmoussa Samir, Bin Jardan Yousef A., Bourhia Mohammed, Salamatullah Ahmad Mohammad, Dauelbait Musaab
Publikováno v:
Open Chemistry, Vol 22, Iss 1, Pp 945-53 (2024)
Solubility enhancement of poorly aqueous-soluble drugs, like Terbinafine (TBN), is a critical challenge in formulating effective dosage forms. This study focused on developing β-cyclodextrin (β-CD) and polyacrylamide (PAM)-based microgels to addres
Externí odkaz:
https://doaj.org/article/151232dd0bfc423cb9fdd9847939ba07
Autor:
Zahra Sohani, Shahram Jamshidi, Mohammad Kazem Koohi, Javad Malakootikhah, Mohammad Abarkar, Diba Golchin, Sarina Roshani, Haniyeh Naghdi, Negin Aghajanpour-moghaddam-gazafroudi, Gazafroudi, Nava Amjadi, Reihaneh Izadi-niaki
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-14 (2024)
Abstract Corneal ulcers, whether melting or indolent, are common in humans and companion animals. Treatment involves local administration of antibiotic eye drops and corneal healing drugs. Compared to traditional treatments for ulcerative keratitis,
Externí odkaz:
https://doaj.org/article/601d5947ca214fcbadbdc44f7e0a3ba6
Publikováno v:
ESPOCH Congresses, Vol 3, Iss 4, Pp 189-206 (2024)
Abstract Bacterial growth in fruits and vegetables causes a large percentage of the loss and waste of these foods worldwide. For this reason, the objective of this study was to develop antibacterial gels based on sodium alginate, β -cyclodextrin, an
Externí odkaz:
https://doaj.org/article/518ad84dadc9477e890218e501764247
Autor:
Otake H, Kobayashi K, Kadowaki R, Kosaka T, Itahashi M, Tsubaki M, Matsuda M, Iwakiri N, Harata E, Nagai N
Publikováno v:
Drug Design, Development and Therapy, Vol Volume 18, Pp 4345-4358 (2024)
Hiroko Otake,1,* Ko Kobayashi,2,* Reita Kadowaki,1 Taiyo Kosaka,1 Mizuki Itahashi,1 Masanobu Tsubaki,1 Masaru Matsuda,2 Norio Iwakiri,2 Eiji Harata,2 Noriaki Nagai1 1Faculty of Pharmacy, Kindai University, Osaka, Japan; 2Life Science Division
Externí odkaz:
https://doaj.org/article/7b5f18c73f954799b65a36642b6e7205
Autor:
Phanit Songvut, Tussapon Boonyarattanasoonthorn, Nitra Nuengchamnong, Thammaporn Junsai, Teetat Kongratanapasert, Kittitach Supannapan, Phisit Khemawoot
Publikováno v:
Pharmaceutical Biology, Vol 62, Iss 1, Pp 183-194 (2024)
AbstractContext The therapeutic potential of andrographolide is hindered by its poor oral bioavailability and unpredictable pharmacokinetics, primarily due to its limited water solubility.Objective This work aimed to enhance the solubility and pharma
Externí odkaz:
https://doaj.org/article/de284fc8644d456296bd8b5e8bf61ac4
Autor:
Anjan Kumar Mahapatra, Siddharth Dora, Sanatan Parida, Usharani Bal, Bandana Rani Jena, Madhusmita Lenka
Publikováno v:
Journal of Applied Pharmaceutical Research, Vol 12, Iss 4, Pp 21-30 (2024)
Background: The work was intended to enhance etoricoxib's solubility and dissolution rate and then develop oro-dispersible tablets for faster onset of action. Methodology: Inclusion complexes (ICs) of the drug were obtained with β-cyclodextrin (β-C
Externí odkaz:
https://doaj.org/article/948cdc25d6d247699c2522f17621ad83
Publikováno v:
Future Journal of Pharmaceutical Sciences, Vol 10, Iss 1, Pp 1-15 (2024)
Abstract Background In advanced or metastatic cancers characterized by specific genetic alterations, heightened growth and resistance to conventional therapies are common. Targeted treatments like entrectinib (ENT) precisely inhibit aberrant signalin
Externí odkaz:
https://doaj.org/article/0d79f4cbfa594c148f48c21167c5ca7c
Autor:
Yanqun XU, Jing HUANG, Ziqing WU, Nanfeng TAN, Jiayi XU, Jia CHEN, Tian YE, Gennü WANG, Dan LONG, Yongquan XU, Zisheng LUO
Publikováno v:
Shipin gongye ke-ji, Vol 45, Iss 16, Pp 129-137 (2024)
Oolong tea was highly favored by consumers for its rich aroma. However, there was significant loss of fragrance in Oolong tea products during processing and storage, urgently necessitating the development of corresponding technologies to stabilize ar
Externí odkaz:
https://doaj.org/article/2aaf2bf7fe8c462ab2a45acb49d14920
Autor:
Shengpeng ZHANG, Genyi ZHANG
Publikováno v:
Shipin gongye ke-ji, Vol 45, Iss 13, Pp 99-107 (2024)
Rutin has a variety of pharmacological activities, in order to solve the application defects caused by its poor water solubility. In this paper, rutin/hydroxypropyl-β-cyclodextrin (HPCD) inclusion complexes were prepared by solvent evaporation metho
Externí odkaz:
https://doaj.org/article/5f154fa99efa4fdbb811d20d2292da12
Publikováno v:
European Pharmaceutical Journal, Vol 71, Iss 1, Pp 32-42 (2024)
The objective of the present investigation is to improve the solubility of valsartan and prepare immediate release tablets.
Externí odkaz:
https://doaj.org/article/dff7919a714b47f59bc035b34b83eb8d