Article(id=1309634592739517347, tenantId=1146029695717560320, journalId=1227999776411738115, issueId=1309634582362809158, articleNumber=null, orderNo=null, doi=10.12048/j.issn.1674-229X.2026.04.010, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1770307200000, receivedDateStr=2026-02-06, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1790170818742, onlineDateStr=2026-09-23, pubDate=1777046400000, pubDateStr=2026-04-25, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1790170818742, onlineIssueDateStr=2026-09-23, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1790170818742, creator=13701087609, updateTime=1790170818742, updator=13701087609, issue=Issue{id=1309634582362809158, tenantId=1146029695717560320, journalId=1227999776411738115, year='2026', volume='36', issue='4', pageStart='241', pageEnd='320', issueExtLink='null', onlineDate='null', pubDate='1777046400000', pubDateStr='2026-04-25', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1790170816268, creator='13701087609', updateTime=1790219015105, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1309836742979576497, tenantId=1146029695717560320, journalId=1227999776411738115, issueId=1309634582362809158, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1309836742979576498, tenantId=1146029695717560320, journalId=1227999776411738115, issueId=1309634582362809158, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=308, endPage=314, ext={EN=ArticleExt(id=1309634592907289508, articleId=1309634592739517347, tenantId=1146029695717560320, journalId=1227999776411738115, language=EN, title=Individualized Dosing Regimens of Teicoplanin for Patients with Hypoalbuminemia Based on Population Pharmacokinetics, columnId=null, journalTitle=Pharmacy Today, columnName=null, runingTitle=null, highlight=null, articleAbstract=
OBJECTIVE

To characterize the pharmacokinetic characteristics of teicoplanin in patients with hypoalbuminemia, explore the target values of pharmacokinetic/pharmacodynamic (PK/PD) parameters, and develop individualized dosing regimens.

METHODS

Clinical data of patients with hypoalbuminemia were retrospectively collected, and a population pharmacokinetic analysis was performed using a nonlinear mixed-effects model. Classification and regression tree (CART) analysis and survival analysis were used to explore and verify the impact of the target values of (PK/PD) parameters on therapeutic efficacy. Monte Carlo simulation was applied to develop individualized dosing regimens.

RESULTS

A one-compartment population pharmacokinetic model of teicoplanin was established using 328 blood concentration values from 195 patients. The population typical values of clearance and apparent volume of distribution of the model were 0.612 L·h-1 and 91.2 L, respectively. Estimated glomerular filtration rate (eGFR) was included as a covariate for clearance, and albumin and urea were included as covariates for the apparent volume of distribution. The target values of PK/PD parameters were determined as trough concentration ≥15 mg·L-1 and the ratio of 24 hour area under the drug-time curve to minimum inhibitory concentration (AUC24/MIC)≥790. Several individualized dosing regimens were developed based on different levels of the model covariates.

CONCLUSION

For patients with hypoalbuminemia receiving teicoplanin, it is necessary to increase the dosage and frequency of the loading dose regimen according to the patients' albumin and eGFR levels, and adjust the maintenance dose regimen according to the MIC of pathogenic bacteria, so as to improve clinical efficacy.

, authors=Jianpeng HE1, 2, Chen YE1, Ying WANG1, Zhanhua HU1, Zeyuan HE1, Yuqing CHEN1, Guocheng LI1, Min HUANG2, Xiaoxia YU1, *, authorsList=Jianpeng HE, Chen YE, Ying WANG, Zhanhua HU, Zeyuan HE, Yuqing CHEN, Guocheng LI, Min HUANG, Xiaoxia YU, authorCompany=null, correspAuthors=Xiaoxia YU, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1309634593272193957, articleId=1309634592739517347, tenantId=1146029695717560320, journalId=1227999776411738115, language=CN, title=基于群体药动学的替考拉宁在低白蛋白血症患者中的个体化用药研究, columnId=1228268588277105398, journalTitle=今日药学, columnName=临床药学, runingTitle=null, highlight=null, articleAbstract=
目的

明确替考拉宁在低白蛋白血症患者中的药动学特征,探索药动学/药效学参数的目标值,制定个体化给药方案。

方法

回顾性收集低白蛋白血症患者的临床数据,使用非线性混合效应模型进行群体药动学分析。使用分类与回归树和生存分析,探索并验证药动学/药效学参数的目标值对疗效的影响。使用蒙特卡洛模拟制定个体化给药方案。

结果

使用195例患者的328个血药浓度值,建立了替考拉宁的一房室群体药动学模型。模型的清除率和表观分布容积的群体典型值分别为0.612 L·h-1和91.2 L,纳入肾小球滤过率作为清除率的协变量,白蛋白和尿素作为表观分布容积的协变量。确定谷浓度≥15 mg·L-1和24 h药时曲线下面积与最小抑菌浓度的比值(AUC24/MIC)≥790为药动学/药效学参数的目标值。基于模型协变量的不同水平,制定了多种个体化给药方案。

结论

低白蛋白血症患者使用替考拉宁时,需根据患者的白蛋白和肾小球滤过率水平,提高负荷剂量方案的用量和次数,并根据病原菌的最小抑菌浓度,调整维持剂量方案,以提高临床疗效。

, authors=何健鹏1, 2, 叶晨1, 王莹1, 胡展华1, 何泽源1, 陈雨晴1, 李国成1, 黄民2, 余晓霞1, *, authorsList=何健鹏, 叶晨, 王莹, 胡展华, 何泽源, 陈雨晴, 李国成, 黄民, 余晓霞, authorCompany=null, correspAuthors=余晓霞, authorNote=

何健鹏,硕士研究生,研究方向:临床药学

, correspAuthorsNote=

*

余晓霞,主任药师,研究方向:临床药学,E-mail:
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基于群体药动学的替考拉宁在低白蛋白血症患者中的个体化用药研究
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何健鹏 1, 2 , 叶晨 1 , 王莹 1 , 胡展华 1 , 何泽源 1 , 陈雨晴 1 , 李国成 1 , 黄民 2 , 余晓霞 1, *
今日药学 | 临床药学 2026,36(4): 308-314
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今日药学 |临床药学 2026 , 36 (4) : 308 -314
基于群体药动学的替考拉宁在低白蛋白血症患者中的个体化用药研究
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何健鹏1, 2, 叶晨1, 王莹1, 胡展华1, 何泽源1, 陈雨晴1, 李国成1, 黄民2, 余晓霞1, *
作者信息
  • 1.中山大学孙逸仙纪念医院药学部,广东 广州 510120
  • 2.中山大学药学院,广东 广州 510006
通讯作者:

*

余晓霞,主任药师,研究方向:临床药学,E-mail:
作者简介:

何健鹏,硕士研究生,研究方向:临床药学

Individualized Dosing Regimens of Teicoplanin for Patients with Hypoalbuminemia Based on Population Pharmacokinetics
Jianpeng HE1, 2, Chen YE1, Ying WANG1, Zhanhua HU1, Zeyuan HE1, Yuqing CHEN1, Guocheng LI1, Min HUANG2, Xiaoxia YU1, *
Affiliations
  • 1.Department of Pharmacy, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, Guangdong 510120, China
  • 2.School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, Guangdong 510006, China
出版时间: 2026-04-25 doi: 10.12048/j.issn.1674-229X.2026.04.010
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目的

明确替考拉宁在低白蛋白血症患者中的药动学特征,探索药动学/药效学参数的目标值,制定个体化给药方案。

方法

回顾性收集低白蛋白血症患者的临床数据,使用非线性混合效应模型进行群体药动学分析。使用分类与回归树和生存分析,探索并验证药动学/药效学参数的目标值对疗效的影响。使用蒙特卡洛模拟制定个体化给药方案。

结果

使用195例患者的328个血药浓度值,建立了替考拉宁的一房室群体药动学模型。模型的清除率和表观分布容积的群体典型值分别为0.612 L·h-1和91.2 L,纳入肾小球滤过率作为清除率的协变量,白蛋白和尿素作为表观分布容积的协变量。确定谷浓度≥15 mg·L-1和24 h药时曲线下面积与最小抑菌浓度的比值(AUC24/MIC)≥790为药动学/药效学参数的目标值。基于模型协变量的不同水平,制定了多种个体化给药方案。

结论

低白蛋白血症患者使用替考拉宁时,需根据患者的白蛋白和肾小球滤过率水平,提高负荷剂量方案的用量和次数,并根据病原菌的最小抑菌浓度,调整维持剂量方案,以提高临床疗效。

替考拉宁  /  低白蛋白血症  /  群体药动学  /  药动学/药效学参数  /  个体化给药方案
OBJECTIVE

To characterize the pharmacokinetic characteristics of teicoplanin in patients with hypoalbuminemia, explore the target values of pharmacokinetic/pharmacodynamic (PK/PD) parameters, and develop individualized dosing regimens.

METHODS

Clinical data of patients with hypoalbuminemia were retrospectively collected, and a population pharmacokinetic analysis was performed using a nonlinear mixed-effects model. Classification and regression tree (CART) analysis and survival analysis were used to explore and verify the impact of the target values of (PK/PD) parameters on therapeutic efficacy. Monte Carlo simulation was applied to develop individualized dosing regimens.

RESULTS

A one-compartment population pharmacokinetic model of teicoplanin was established using 328 blood concentration values from 195 patients. The population typical values of clearance and apparent volume of distribution of the model were 0.612 L·h-1 and 91.2 L, respectively. Estimated glomerular filtration rate (eGFR) was included as a covariate for clearance, and albumin and urea were included as covariates for the apparent volume of distribution. The target values of PK/PD parameters were determined as trough concentration ≥15 mg·L-1 and the ratio of 24 hour area under the drug-time curve to minimum inhibitory concentration (AUC24/MIC)≥790. Several individualized dosing regimens were developed based on different levels of the model covariates.

CONCLUSION

For patients with hypoalbuminemia receiving teicoplanin, it is necessary to increase the dosage and frequency of the loading dose regimen according to the patients' albumin and eGFR levels, and adjust the maintenance dose regimen according to the MIC of pathogenic bacteria, so as to improve clinical efficacy.

teicoplanin  /  hypoalbuminemia  /  population pharmacokinetics  /  pharmacokinetic/pharmacodynamic (PK/PD) parameters  /  individualized dosing regimens
何健鹏, 叶晨, 王莹, 胡展华, 何泽源, 陈雨晴, 李国成, 黄民, 余晓霞. 基于群体药动学的替考拉宁在低白蛋白血症患者中的个体化用药研究. 今日药学, 2026 , 36 (4) : 308 -314 . DOI: 10.12048/j.issn.1674-229X.2026.04.010
Jianpeng HE, Chen YE, Ying WANG, Zhanhua HU, Zeyuan HE, Yuqing CHEN, Guocheng LI, Min HUANG, Xiaoxia YU. Individualized Dosing Regimens of Teicoplanin for Patients with Hypoalbuminemia Based on Population Pharmacokinetics[J]. Pharmacy Today, 2026 , 36 (4) : 308 -314 . DOI: 10.12048/j.issn.1674-229X.2026.04.010
  • 广东省药学会科学研究基金(2024A28)
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doi: 10.12048/j.issn.1674-229X.2026.04.010
  • 接收时间:2026-02-06
  • 首发时间:2026-09-23
  • 出版时间:2026-04-25
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  • 收稿日期:2026-02-06
基金
广东省药学会科学研究基金(2024A28)
作者信息
    1.中山大学孙逸仙纪念医院药学部,广东 广州 510120
    2.中山大学药学院,广东 广州 510006

通讯作者:

*

余晓霞,主任药师,研究方向:临床药学,E-mail:
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2种不同金属材料的力学参数
科
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属数
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genus
种数
Number of
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占总种数比例
Percentage of
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属
Genus
种数
Number of
species
占总种数比例
Percentage of total
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鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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