2019
DOI: 10.1002/bmc.4561
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Pharmacokinetics of salvianolic acid B, rosmarinic acid and Danshensu in rat after pulmonary administration of Salvia miltiorrhiza polyphenolic acid solution

Abstract: A sensitive and accurate LC-MS/MS method was established for quantifying salvianolic acid B (Sal B), rosmarinic acid (Ros A) and Danshensu (DA) in rat plasma. Salvia miltiorrhiza polyphenolic acid (SMPA), active water-soluble ingredients isolated and purified from Salvia miltiorrhiza Bge included Sal B, Ros A and DA. The pharmacokinetic analysis of Sal B, Ros A and DA after pulmonary administration of SMPA solution to rat was performed by LC-MS/MS. Results from the pharmacokinetic studies showed that the peak … Show more

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Cited by 25 publications
(15 citation statements)
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“…RA could be rapidly eliminated from rat plasma collected at 4 and 8 h after the intravenous and oral administration, with elimination half-lives (t 1/2 ) of 0.67 ± 0.24 and 1.34 ± 0.22 h, respectively. Compared with previous reports (Lu et al, 2019;Yang et al, 2018) which targeted the in vivo process of TCM preparation or herbal extract, some of the pharmacokinetic parameters of RA determined were different to some extent, such as t 1/2 and t max . On the one hand, TCM preparations can affect the release and dissolution rate of small molecule compounds in the gastrointestinal tract, and on the other hand, drug-drug interactions may occur when RA and other components are intravenously or orally administrated together.…”
Section: Pharmacokinetics Studycontrasting
confidence: 76%
“…RA could be rapidly eliminated from rat plasma collected at 4 and 8 h after the intravenous and oral administration, with elimination half-lives (t 1/2 ) of 0.67 ± 0.24 and 1.34 ± 0.22 h, respectively. Compared with previous reports (Lu et al, 2019;Yang et al, 2018) which targeted the in vivo process of TCM preparation or herbal extract, some of the pharmacokinetic parameters of RA determined were different to some extent, such as t 1/2 and t max . On the one hand, TCM preparations can affect the release and dissolution rate of small molecule compounds in the gastrointestinal tract, and on the other hand, drug-drug interactions may occur when RA and other components are intravenously or orally administrated together.…”
Section: Pharmacokinetics Studycontrasting
confidence: 76%
“…As above-mentioned, RA often serves as an indicator for the quality evaluation of some folk herbal medicines or compound medicines. In the same way, RA also acts as a representative component in the pharmacokinetic studies of these medicines such as the Salvia miltiorrhiza polyphenolic acid solution [ 286 ], Prunella vulgaris extract [ 287 ], ZibuPiyin Recipe [ 288 ], and Xuebijing Injection [ 289 ]. Table 2 presents the specific parameters of these pharmacokinetic studies including the AUC (0 → ∞) , T max , C max , and CL.…”
Section: Pharmacokineticsmentioning
confidence: 99%
“…Macrophages profoundly altered the balance between destructive tissue remodeling and reparative tissue healing through their role in both promotion and resolution of the inflammatory response (Dale et al, 2016). NF‐κB signaling pathway is mainly composed of a series of NF‐κB/Rel proteins, including NF‐κB1, NF‐κB2, p50, p52, c‐Rel, Rel A (p65) and Rel B (P. Lu et al, 2019). Some studies reported that NF‐κB inhibitor markedly suppressed the activity of MMP‐2, MMP‐99, MMP‐3 and MMP‐12, and inhibited AAA formation (Shiraya et al, 2006).…”
Section: Discussionmentioning
confidence: 99%