Relevant bibliographies by topics / HP Beta-Cyclodextrin

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Academic literature on the topic 'HP Beta-Cyclodextrin'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "HP Beta-Cyclodextrin"

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Liu, Hui, Jinhua Luo, Ping Yang, Xiulan Yang, Jun Yan, and Qian Yao. "Stability, Antioxidant Activity and Intestinal Permeation of Oleuropein Inclusion Complexes with Beta-Cyclodextrin and Hydroxypropyl-Beta-Cyclodextrin." Molecules 27, no. 16 (2022): 5077. http://dx.doi.org/10.3390/molecules27165077.

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Compared to beta-cyclodextrins (beta-CD), hydroxypropyl-beta-cyclodextrins (HP-beta-CD) are a more popular material used to prepare inclusion complexes due to their superior solubility and intestinal absorption. In this study, oleuropein (OL) inclusion complexes with beta-CD (beta-CD:OL) and HP-beta-CD (HP-beta-CD:OL) were prepared and the formation of inclusion complexes was validated by IR, PXRD, and DSC. A phase solubility test showed that the lgK (25 °C) and binding energy of beta-CD:OL and HP-beta-CD:OL was 2.32 versus 1.98, and −6.1 versus −24.66 KJ/mol, respectively. Beta-CD:OL exhibite
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Abhijit, Banik, та Dutta Saikia Monali. "Triflumizole encapsulation by 2-hydroxypropyl and sulphated derivatives of β-cyclodextrin". Journal of Indian Chemical Society Vol. 91, May 2014 (2014): 865–70. https://doi.org/10.5281/zenodo.5720090.

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Department of Chemistry, Arya Vidyapeeth College, Guwahati-781 016, Assam, India <em>E-mail</em> : monalisaikia@hotmail.com Fax : 91-361-244065 <em>Manuscript received online 07 March 2013, revised 27 June 2013, accepted 28 June 2013</em> Spectroscopic studies were done on the inclusion of triflumizole (TF) into the cavities of two derivatives of &beta;-cyclodextrin namely hydroxypropyl-&beta;-cyclodextrin (HP-&beta;-CD) and sulphated-&beta;-cyclodextrin (S-&beta;-CD). The affinity of TF for the cavities of cyclodextrin derivatives was found to be dependent on the interaction forces responsibl
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Wang, Runmiao, Hui Zhou, Shirley W. I. Siu, Yong Gan, Yitao Wang, and Defang Ouyang. "Comparison of Three Molecular Simulation Approaches for Cyclodextrin-Ibuprofen Complexation." Journal of Nanomaterials 2015 (2015): 1–8. http://dx.doi.org/10.1155/2015/193049.

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Cyclodextrins are widely used for the solubilisation of poorly soluble drugs in the formulations. However, current cyclodextrin formulation development strongly depends on trial-and-error in the laboratory, which is time-consuming and high cost. The aim of this research was to compare three modeling approaches (Docking, molecular dynamics (MD), and quantum mechanics (QM)) for cyclodextrin/drug complexation. Ibuprofen was used as a model drug. Binding free energy from three simulation methods was calculated as an important parameter to compare with the experimental results. Docking results from
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Lv, Junli, Jiali Zou, Jianjiao Niu, and Guoze Wang. "Evaluation of orally disintegrating films containing ferulic acid inclusion complexes: Physical characteristics and release kinetics." Emirates Journal of Food and Agriculture 37 (June 30, 2025): 1–10. https://doi.org/10.3897/ejfa.2025.152376.

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Orally disintegrating films (ODFs) has gained significant attention as a nutrient delivery platform due to its ease of intake. But studies on delivering ferulic acid (FA) through ODFs are still scarce. The objective of this study was to assess the physical characteristics of ODFs containing FA/&amp;beta;-cyclodextrin (0.5:1) (FA/&amp;beta;-CD (0.5:1)) and FA/hydroxypropyl-&amp;beta;-cyclodextrin (0.5:1) (FA/HP-&amp;beta;-CD (0.5:1)) complexes, as well as analyze the release kinetics of FA in both ODFs. Confirmation of the FA/&amp;beta;-CD (0.5:1) and FA/HP-&amp;beta;-CD (0.5:1) inclusion compl
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Székely-Szentmiklósi, Blanka, and B. Tőkés. "Study of Cyclodextrin/Fluoroquinolone Inclusion Complexes by Capillary Electrophoresis." Acta Medica Marisiensis 59, no. 2 (2013): 107–10. http://dx.doi.org/10.2478/amma-2013-0026.

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AbstractIntroduction: In the present work we evaluated the complexation role of cyclodextrins toward fluoroquinolones in an attempt to assess their potential as new formulation additives for more efficient fluoroquinolone delivery and as selectors in capillary electrophoresis.Material and method: Guest-host interactions of two second generation quinolones, ciprofloxacin and norfloxacin with four cyclodextrins, beta-cyclodextrin (β-CD), gamma-cyclodextrin (γ-CD) and two beta-cyclodextrin derivatives, 2-hydroxypropyl beta-cyclodextrin (HP-β-CD) and randomly methylated beta-cyclodextrin (RAMEB),
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Kuzmanović Nedeljković, Snežana, Milica Radan, Dubravka Bigović, and Katarina Šavikin. "Cyclodextrin-aided green extraction from Fagopyrum esculentum Moench – an effective strategy for the sustainable recovery of polyphenols." Lekovite sirovine 44, no. 1 (2024): 1–9. https://doi.org/10.61652/leksir2444012k.

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&amp;lt;p&amp;gt;As a rich source of polyphenolic compounds, &amp;lt;em&amp;gt;Fagopyrum esculentum &amp;lt;/em&amp;gt;Moench herb, is a valuable subject for a numerous industries, such as pharmaceutical, chemical, food, or cosmetic. Given the biological potential that is closely related to the polyphenolic content, this study aimed to develop ecologically suitable cyclodextrin-aided extraction from the aerial parts of &amp;lt;em&amp;gt;F. esculentum&amp;lt;/em&amp;gt;. To maximize the polyphenolic content, highly-reliable mathematical and statistical method &amp;amp;ndash; response surface me
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Pal, Kaushik, Falguni Chandra, Suman Mallick та Apurba L. Koner. "pH dependent supramolecular recognition of dapoxyl sodium sulfonate with 2-hydroxypropyl β-cyclodextrin: an application towards food-additive formulation". New Journal of Chemistry 40, № 7 (2016): 6093–100. http://dx.doi.org/10.1039/c5nj03415a.

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Ozon, Emma Adriana, Marian Novac, Daniela Gheorghe та ін. "Formation and Physico-Chemical Evaluation of Nifedipine-hydroxypropyl-β-cyclodextrin and Nifedipine-methyl-β-cyclodextrin: The Development of Orodispersible Tablets". Pharmaceuticals 15, № 8 (2022): 993. http://dx.doi.org/10.3390/ph15080993.

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The novelty in this study is the development of new orodispersible tablets containing nifedipine (NIF) as the active ingredient. Initially, the formation of inclusion complexes between nifedipine and two derivatives of beta-cyclodextrin, namely, hydroxypropyl-β-cyclodextrin (HP-β-CD) and methyl-β-cyclodextrin (Me-β-CD), was established. Inclusion complexes of nifedipine were prepared by different procedures: kneading, coprecipitation and lyophilization methods, using a 1:1 molar ratio among the drug and cyclodextrin compounds. A physical mixture was also developed for comparison, with the same
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Paczkowska-Walendowska, Magdalena, Jakub Dvorák, Natalia Rosiak, et al. "Buccal Resveratrol Delivery System as a Potential New Concept for the Periodontitis Treatment." Pharmaceutics 13 (March 20, 2021): 417. https://doi.org/10.3390/pharmaceutics13030417.

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Abstract: The health benefits of resveratrol have been proven to inhibit the development of numerous diseases. A frequent limitation in its use is a low bioavailability stemming from a poor solubility and fast enterohepatic metabolism. Thus, the aim of the research was to investigate the possibility to formulate mucoadhesive cyclodextrin- and xanthan gum-based buccal tablets in order to increase the solubility of resveratrol and to eliminate bypass enterohepatic metabolism. Systems of resveratrol with alpha-cyclodextrin (alpha-CD), beta-cyclodextrin (beta-CD), gamma-cyclodextrin (gamma-CD) and
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Wu, Hsien-Tsung, Yao-Hsiang Chuang, Han-Cyuan Lin, and Liang-Jung Chien. "Characterization and Aerosolization Performance of HydroxyPropyl-Beta-Cyclodextrin Particles Produced Using Supercritical Assisted Atomization." Polymers 13, no. 14 (2021): 2260. http://dx.doi.org/10.3390/polym13142260.

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In this study, hydroxypropyl-beta-cyclodextrin (HP-β-CD) particles were produced using supercritical assisted atomization (SAA) with carbon dioxide as the spraying medium or co-solute and aqueous ethanol solution as the solvent. The effects of several key factors on the morphology and size of the HP-β-CD particles were investigated. These factors included the solvent effect, temperatures of the precipitator and saturator, concentration of the HP-β-CD solution, and flow rate ratio of carbon dioxide to the HP-β-CD solution. The conducive conditions for producing fine spherical particles were 54.
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Reports on the topic "HP Beta-Cyclodextrin"

1

Tengamnuay, Parkpoom, Achariya Sailasuta, and Garnpimol C. Ritthidej. Efficacy and mechanistic studies of chitosan as nasal absorption enhancer of peptide drugs. Chulalongkorn University, 1998. https://doi.org/10.58837/chula.res.1998.21.

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Objective: To evaluate the safety and efficacy of chitosan (CS) as nasal absorption enhances of peptides. Methods: Two types of chitosans, i.e. CS J (free amine chitosan) and CD G (water-soluble glutamate salt), were evaluate for their masal absorption enhancing effectd on L-Tyr-D-Arg([D-Arg[square]]-Kyotorphic), an enzymatically stable dipeptide, using an in situ rat nasal perfusion technique. The two chitosans were subsequently studies for their possible membrane damaging effects based on measurements of releases mucosal components and histological evaluation. Results: At 0.5% w/v, both CS J
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