Literature DB >> 25986594

Solid-State and Solution Characterization of Myricetin.

Stephen J Franklin1, Paul B Myrdal2.   

Abstract

Myricetin (MYR) is a natural compound that has been investigated as a chemopreventative agent. MYR has been shown to suppresses ultraviolet B (UVB)-induced cyclooxygenase-2 (COX-2) protein expression and reduce the incidence of UVB-induced skin tumors in mice. Despite MYR's promise as a therapeutic agent, minimal information is available to guide the progression of formulations designed for future drug development. Here, data is presented describing the solid-state and solution characterization of MYR. Investigation into the solid-state properties of MYR identified four different crystal forms, two hydrates (MYR I and MYR II) and two metastable forms (MYR IA and MYR IIA). From solubility studies, it was evident that all forms are very insoluble (<5 μg/ml) in pure water. MYR I was found to be the most stable form at 23, 35, and 56°C. Stability determination indicated that MYR undergoes rapid apparent first-order degradation under basic pH conditions, and that degradation was influenced by buffer species. Apparent first-order degradation was also seen when MYR was introduced to an oxidizing solution. Improved stability was achieved after introducing 0.1% antioxidants to the solution. MYR was found to have good stability following exposure to ultraviolet radiation (UVR), which is a consideration for topical applications. Finally, a partitioning study indicated that MYR possess a log P of 2.94 which, along with its solid-state properties, contributes to its poor aqueous solubility. Both the solid-state properties and solution stability of MYR are important to consider when developing future formulations.

Entities:  

Keywords:  hydrate; log P; myricetin; solubility; stability

Mesh:

Substances:

Year:  2015        PMID: 25986594      PMCID: PMC4666259          DOI: 10.1208/s12249-015-0329-6

Source DB:  PubMed          Journal:  AAPS PharmSciTech        ISSN: 1530-9932            Impact factor:   3.246


  18 in total

Review 1.  Stabilization of pharmaceuticals to oxidative degradation.

Authors:  Kenneth C Waterman; Roger C Adami; Karen M Alsante; Jinyang Hong; Margaret S Landis; Franco Lombardo; Christopher J Roberts
Journal:  Pharm Dev Technol       Date:  2002-01       Impact factor: 3.133

Review 2.  Cancer chemoprevention with dietary phytochemicals.

Authors:  Young-Joon Surh
Journal:  Nat Rev Cancer       Date:  2003-10       Impact factor: 60.716

Review 3.  Cellular and molecular events leading to the development of skin cancer.

Authors:  Vladislava O Melnikova; Honnavara N Ananthaswamy
Journal:  Mutat Res       Date:  2005-04-01       Impact factor: 2.433

4.  Formation of isomorphic desolvates: creating a molecular vacuum.

Authors:  G A Stephenson; E G Groleau; R L Kleemann; W Xu; D R Rigsbee
Journal:  J Pharm Sci       Date:  1998-05       Impact factor: 3.534

5.  The validity and practicality of sun-reactive skin types I through VI.

Authors:  T B Fitzpatrick
Journal:  Arch Dermatol       Date:  1988-06

6.  The wavelengths in sunlight effective in producing skin cancer: a theoretical analysis.

Authors:  R B Setlow
Journal:  Proc Natl Acad Sci U S A       Date:  1974-09       Impact factor: 11.205

7.  Content of the flavonols quercetin, myricetin, and kaempferol in 25 edible berries.

Authors:  S H Häkkinen; S O Kärenlampi; I M Heinonen; H M Mykkänen; A R Törrönen
Journal:  J Agric Food Chem       Date:  1999-06       Impact factor: 5.279

8.  Determination of stilbenes (trans-astringin, cis- and trans-piceid, and cis- and trans-resveratrol) in Portuguese wines.

Authors:  M T Ribeiro de Lima; P Waffo-Téguo; P L Teissedre; A Pujolas; J Vercauteren; J C Cabanis; J M Mérillon
Journal:  J Agric Food Chem       Date:  1999-07       Impact factor: 5.279

9.  Dietary antioxidant flavonoids and risk of coronary heart disease: the Zutphen Elderly Study.

Authors:  M G Hertog; E J Feskens; P C Hollman; M B Katan; D Kromhout
Journal:  Lancet       Date:  1993-10-23       Impact factor: 79.321

10.  Fast- and slow-release tablets for oral administration of flavonoids: rutin and quercetin.

Authors:  Maria Rosaria Lauro; Maria Luisa Torre; Lauretta Maggi; Francesco De Simone; Ubaldo Conte; Rita Patrizia Aquino
Journal:  Drug Dev Ind Pharm       Date:  2002-04       Impact factor: 3.225

View more
  4 in total

1.  Estimating the Aqueous Solubility of Pharmaceutical Hydrates.

Authors:  Stephen J Franklin; Usir S Younis; Paul B Myrdal
Journal:  J Pharm Sci       Date:  2016-06       Impact factor: 3.534

2.  New micelle myricetin formulation for ocular delivery: improved stability, solubility, and ocular anti-inflammatory treatment.

Authors:  Fengyuan Sun; Zhou Zheng; Jie Lan; Xuefei Li; Mengshuang Li; Kaichao Song; Xianggen Wu
Journal:  Drug Deliv       Date:  2019-12       Impact factor: 6.419

3.  Solubility Enhancement of Myricetin by Inclusion Complexation with Heptakis-O-(2-Hydroxypropyl)-β-Cyclodextrin: A Joint Experimental and Theoretical Study.

Authors:  Dongxu Han; Zhongbao Han; Liyan Liu; Ying Wang; Shigang Xin; Hongbo Zhang; Zhan Yu
Journal:  Int J Mol Sci       Date:  2020-01-24       Impact factor: 5.923

4.  Chemoprevention of intestinal tumorigenesis by the natural dietary flavonoid myricetin in APCMin/+ mice.

Authors:  Ye Li; Shu-Xiang Cui; Shi-Yue Sun; Wen-Na Shi; Zhi-Yu Song; Shu-Qing Wang; Xin-Feng Yu; Zu-Hua Gao; Xian-Jun Qu
Journal:  Oncotarget       Date:  2016-09-13
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.