Preparation, characterization, and toxicity evaluation of microemulsion formulation containing prunetin for potential oral applications

被引:2
作者
Karayildirim, Cinel Koksal [1 ]
Okur, Neslihan Ustundag [2 ]
Okur, Mehmet Evren [3 ]
Caglar, Emre Sefik [4 ]
Nalbantsoy, Ayse [5 ]
Alsakini, Karar Ali Mohammed Hasan [5 ]
Yavasoglu, Nefise Ulku Karabay [1 ]
机构
[1] Ege Univ, Fac Sci, Dept Biol, TR-35100 Izmir, Turkiye
[2] Univ Hlth Sci, Fac Pharm, Dept Pharmaceut Technol, Istanbul, Turkiye
[3] Univ Hlth Sci, Fac Pharm, Dept Pharmacol, Istanbul, Turkiye
[4] Univ Hlth Sci, Fac Pharm, Dept Pharmaceut Biotechnol, Istanbul, Turkiye
[5] Ege Univ, Fac Engn, Dept Bioengn, Izmir, Turkiye
关键词
Isoflavones; prunetin; microemulsion; cytokines; acute oral toxicity; MACROPHAGES; ABSORPTION; EXPRESSION; SURFACTANT; CYTOKINES; PEPTIDE; LPS;
D O I
10.1080/01480545.2023.2282373
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Phytochemicals as therapeutic alternatives can have a fundamental impact on the various stages of inflammation and its resolution. Prunetin is a naturally occurring isoflavone and has been claimed to have numerous therapeutic potentials. The objective of this study is preparation, characterization, and toxicity evaluation of microemulsion formulation containing prunetin (PMF) for potential oral applications. With this research, it was targeted to emphasize the way of improving the therapeutic efficacy of natural biomolecules with a nontoxic and effective formulation. In the study, the pseudo-ternary phase diagram was developed and PMF was characterized by conductivity, droplet size, viscosity and pH. Effects against to cytokines (IL-1 beta and IL-6) and TNF-alpha levels of the PMF were determined by ELISA technique. Genotoxicity and acute oral toxicity tests were carried out according to OECD guidelines. The results showed that PMF is a colloid system that reduced proinflammatory cytokine levels in LPS-induced macrophage cells compared to the control group. PMF demonstrated no mutagenic activity against TA98, TA100, TA1535, and TA1537 Salmonella strains. The in vivo oral acute toxicity test results indicated that PMF did not show mortality or significant side effects even at 2000 mg/kg bw. This study represents PMF showed a good safety profile in animal study. It is thought that this formulation may have anti-inflammatory potential with further in vivo testing.
引用
收藏
页码:235 / 242
页数:8
相关论文
共 50 条
[31]   Formulation and In-vitro Evaluation of Tretinoin Microemulsion as a Potential Carrier for Dermal Drug Delivery [J].
Mortazavi, Seyed Alireza ;
Pishrochi, Sanaz ;
Azar, Zahra Jafari .
IRANIAN JOURNAL OF PHARMACEUTICAL RESEARCH, 2013, 12 (04) :599-609
[32]   Enhanced oral bioavailability of a sterol-loaded microemulsion formulation of Flammulina velutipes, a potential antitumor drug [J].
Yi, Chengxue ;
Zhong, Hui ;
Tong, Shanshan ;
Cao, Xia ;
Firempong, Caleb K. ;
Liu, Hongfei ;
Fu, Min ;
Yang, Yan ;
Feng, Yingshu ;
Zhang, Huiyun ;
Xu, Ximing ;
Yu, Jiangnan .
INTERNATIONAL JOURNAL OF NANOMEDICINE, 2012, 7 :5067-5078
[33]   Aprotinin revisited: formulation, characterization, biodistribution and therapeutic potential of new aprotinin microemulsion in acute pancreatitis [J].
Karasulu, H. Yesim ;
Oruc, Nevin ;
Ustundag-Okur, Neslihan ;
Ozdemir, Derya Ilem ;
Senyigit, Zeynep Ay ;
Yilmaz, Funda Barbet ;
Asikoglu, Makbule ;
Ozkilic, Hayal ;
Akcicek, Eren ;
Guneri, Tamer ;
Ozutemiz, Omer .
JOURNAL OF DRUG TARGETING, 2015, 23 (06) :525-537
[34]   Preparation, characterization, sterility validation, and in vitro cell toxicity studies of microemulsions possessing potential parenteral applications [J].
Nesamony, Jerry ;
Zachar, Carrie L. ;
Jung, Rose ;
Williams, Frederick E. ;
Nauli, Surya .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2013, 39 (02) :240-251
[35]   Preparation, in-vitro release and antioxidant potential of formulation of apigenin with hydroxypropyl-β-cyclodextrin modified microemulsion [J].
Xin Zhao ;
Zhongni Wang ;
Xuepeng Li .
Journal of Inclusion Phenomena and Macrocyclic Chemistry, 2016, 86 :93-102
[36]   Preparation, in-vitro release and antioxidant potential of formulation of apigenin with hydroxypropyl-β-cyclodextrin modified microemulsion [J].
Zhao, Xin ;
Wang, Zhongni ;
Li, Xuepeng .
JOURNAL OF INCLUSION PHENOMENA AND MACROCYCLIC CHEMISTRY, 2016, 86 (1-2) :93-102
[37]   Development and in vitro-in vivo evaluation of a water-in-oil microemulsion formulation for the oral delivery of troxerutin [J].
Xu, Man ;
Yu, Qing ;
Zhao, Qianru ;
Chen, Wei ;
Lin, Yuanjie ;
Jin, Yong .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2016, 42 (02) :280-287
[38]   Formulation development and in vitro evaluation of solidified self-microemulsion in the form of tablet containing atorvastatin calcium [J].
Ali, Kazi Asraf ;
Mukherjee, Biswajit ;
Bandyopadhyay, Amal Kumar .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2013, 39 (11) :1742-1749
[39]   Enhanced anti-cataract effect of microemulsion containing Cineraria maritima: Formulation, optimization and in vivo evaluation [J].
Durgapal, Sumit ;
Goswami, Laxmi ;
Nair, Anroop B. ;
Juyal, Vijay ;
Verma, Anurag .
JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY, 2022, 77
[40]   Optimization of Brinzolamide Loaded Microemulsion Using Formulation by Design Approach: Characterization and In-vitro Evaluation [J].
Gohil, Riyaz ;
Patel, Asha ;
Pandya, Tosha ;
Dharamsi, Abhay .
CURRENT DRUG THERAPY, 2020, 15 (01) :37-52