Results 191 to 200 of about 8,021 (203)
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Tanshinone IIA: Pharmacology, Total Synthesis, and Progress in Structure-modifications
Current Medicinal Chemistry, 2022: Tanshinone IIA, a major bioactive constituent of Danshen, a Chinese herbal medicine, has gained extensive exploration owing to its unique structural features and multiple promising biological activities. This review focuses on the pharmacology, total synthesis, and structural modifications of tanshinone IIA.
Xing, Huang +3 more
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Effects and mechanisms of tanshinone IIA on PTSD-like symptoms
Phytomedicine, 2023In recent years, Salvia miltiorrhiza and its active substances have remarkably progressed in treating central neurological disorders. Tanshinone IIA (TSA) is an active ingredient derived from the rhizome of Salvia miltiorrhiza that has been found to alleviate the symptoms of several psychiatric illnesses.
Kai-Bin Hu +8 more
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Preparation, Characterization and Cytotoxicity Evaluation of Tanshinone IIA Nanoemulsions
Journal of Biomedical Nanotechnology, 2011Tanshinone IIA (TA) is a major active component of Danshen (Salvia miltiorrhiza bunge), a well-known traditional Chinese medicine. In this paper, we describe an optimal method for preparing TA nanoemulsions (TA-NEs) to solve the problems of TA's poor solubility in water and insufficient dissolution rate.
Li-Ching, Chang +5 more
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Advanced Materials Research, 2013
In this study, Tanshinone IIA lipid microspere (Tan-IIA-LM) was successfully prepared by an ultrasonic and high-pressure homogenization method. The particle size, zeta potential, drug entrapment efficiency and morphological properties of Tan-IIA-LM were characterized in detail.
Xin Li Liang +6 more
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In this study, Tanshinone IIA lipid microspere (Tan-IIA-LM) was successfully prepared by an ultrasonic and high-pressure homogenization method. The particle size, zeta potential, drug entrapment efficiency and morphological properties of Tan-IIA-LM were characterized in detail.
Xin Li Liang +6 more
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Chemical Communications, 2017
An easily self-assembled and gelated octa-peptide FHFDFHFD was chosen as a novel drug delivery system (DDS) for both tanshinone IIA and total tanshinone extract.
Yajun, Yin +5 more
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An easily self-assembled and gelated octa-peptide FHFDFHFD was chosen as a novel drug delivery system (DDS) for both tanshinone IIA and total tanshinone extract.
Yajun, Yin +5 more
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Potential anticancer activity of tanshinone IIA against human breast cancer
International Journal of Cancer, 2005Tanshinone IIA is a derivative of phenanthrene-quinone isolated from Danshen, a widely used Chinese herbal medicine. It has antioxidant properties and cytotoxic activity against multiple human cancer cell lines, inducing apoptosis and differentiation of some human cancer cell lines.
Xiujie, Wang +6 more
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Sodium Tanshinone IIA sulfonate improves post-ischemic angiogenesis in hyperglycemia
Biochemical and Biophysical Research Communications, 2019Diabetes is a strong risk factor of peripheral arterial disease (PAD), and also leads to impaired perfusion recovery in the ischemic limb, which eventually results in poor outcomes in PAD patients. Sodium Tanshinone IIA Sulfonate (STS), a monomer from herbs, has been shown to improve the outcomes in a variety of ischemic disease including myocardial ...
Lingdan, Chen +7 more
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Tanshinone IIA Improves Intestinal Barrier Integrity in Septic Rats
Surgical InfectionsAims: The present work aimed to examine impact of tanshinone IIA on intestinal barrier in sepsis and to explore the underpinning mechanisms. Materials and Methods: Sepsis induction in Sprague-Dawley (SD) rats was conducted via cecal ligation and puncture (CLP), with subsequent intraperitoneal injection of tanshinone IIA.
Lvzhao, Liao +8 more
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[Study on the chemical stability of tanshinone IIA].
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 2011To investigate the chemical kinetics of tanshinone IIA in different conditions quantitatively and calculate the chemical kinetic parameters and equations in order to find out the major factors affecting the stability of tanshinone IIA.The kinetic line was obtained by setting the ln (C(t)/C0) as ordinate and making time as abscissa.
Mei, Liu, Xin-Hua, Xia
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