carbamazepine (BioDeep_00000398948)

Main id: BioDeep_00000001445

 

natural product


代谢物信息卡片


Carbamazepine (Carbatrol)

化学式: C15H12N2O (236.095)
中文名称: 卡马西平
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1=CC=C2C(=C1)C=CC3=CC=CC=C3N2C(=O)N
InChI: InChI=1S/C15H12N2O/c16-15(18)17-13-7-3-1-5-11(13)9-10-12-6-2-4-8-14(12)17/h1-10H,(H2,16,18)

描述信息

D002492 - Central Nervous System Depressants > D014149 - Tranquilizing Agents > D018692 - Antimanic Agents
D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D014149 - Tranquilizing Agents
N - Nervous system > N03 - Antiepileptics > N03A - Antiepileptics > N03AF - Carboxamide derivatives
D065693 - Cytochrome P-450 Enzyme Inducers > D065701 - Cytochrome P-450 CYP3A Inducers
D002491 - Central Nervous System Agents > D002492 - Central Nervous System Depressants
COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials
D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents
C78272 - Agent Affecting Nervous System > C264 - Anticonvulsant Agent
D002491 - Central Nervous System Agents > D000927 - Anticonvulsants
D002317 - Cardiovascular Agents > D026941 - Sodium Channel Blockers
D002491 - Central Nervous System Agents > D000700 - Analgesics
D049990 - Membrane Transport Modulators
Corona-virus
Coronavirus
SARS-CoV-2
COVID-19
SARS-CoV
COVID19
SARS2
SARS

同义名列表

3 个代谢物同义名

carbamazepine; Carbamazepine (Carbatrol); Carbamazepine



数据库引用编号

21 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(0)

PlantCyc(0)

代谢反应

0 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

0 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有：

  • PubMed: 来源于PubMed文献库中的文献信息，我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表，这个列表按照代谢物同时出现的文献数量降序排序，取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘，得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序，取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中，存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称，可以跳转到相关代谢物的信息页面。

亚细胞结构定位 关联基因列表
Cytoplasm 5 AXIN2, CYP2C19, CYP2C9, CYP2D6, MTOR
Peripheral membrane protein 1 MTOR
Endosome membrane 1 HLA-A
Endoplasmic reticulum membrane 7 CD4, CYP2C19, CYP2C9, CYP2D6, CYP3A5, HLA-A, MTOR
Mitochondrion membrane 2 ABCG2, TSPO
Nucleus 3 AXIN2, MTOR, NR1I2
cytosol 4 AXIN2, KCNA1, MTOR, TSPO
dendrite 2 KCNA1, MTOR
mitochondrial membrane 2 ABCG2, TSPO
nuclear body 2 NR1I2, SCN1A
phagocytic vesicle 1 MTOR
centrosome 1 AXIN2
nucleoplasm 4 ABCG2, MTOR, NR1I2, SCN1A
Cell membrane 7 ABCG2, CD4, HLA-A, KCNA1, SCN1A, SCN2A, SCN9A
Cytoplasmic side 1 MTOR
Cell projection, axon 2 KCNA1, SCN9A
Early endosome membrane 1 HLA-A
Multi-pass membrane protein 8 ABCC2, ABCG2, CACNA1I, KCNA1, SCN1A, SCN2A, SCN9A, TSPO
Golgi apparatus membrane 1 MTOR
Synapse 1 KCNA1
cell junction 1 KCNA1
cell surface 3 ABCC2, HLA-A, KCNA1
glutamatergic synapse 2 KCNA1, SCN2A
Golgi apparatus 1 HLA-A
Golgi membrane 3 HLA-A, INS, MTOR
lysosomal membrane 2 HLA-A, MTOR
neuronal cell body 2 KCNA1, SCN1A
presynaptic membrane 2 KCNA1, SCN2A
Lysosome 1 MTOR
Presynapse 1 KCNA1
plasma membrane 13 ABCC2, ABCG2, AXIN2, BCHE, CACNA1I, CD4, CYP2C19, CYP2C9, HLA-A, KCNA1, SCN1A, SCN2A, SCN9A
Membrane 12 ABCC2, ABCG2, CACNA1I, CYP2D6, CYP3A5, HLA-A, KCNA1, MTOR, SCN1A, SCN2A, SCN9A, TSPO
apical plasma membrane 3 ABCC2, ABCG2, KCNA1
axon 2 SCN2A, SCN9A
extracellular exosome 3 HLA-A, SHBG, TSPO
Lysosome membrane 2 HLA-A, MTOR
endoplasmic reticulum 4 CYP2D6, HLA-A, KCNA1, TSPO
extracellular space 3 BCHE, HLA-A, INS
intercalated disc 2 SCN1A, SCN2A
intercellular canaliculus 1 ABCC2
mitochondrion 2 CYP2D6, TSPO
intracellular membrane-bounded organelle 5 CYP2C19, CYP2C9, CYP2D6, CYP3A5, TSPO
Microsome membrane 4 CYP2C9, CYP2D6, CYP3A5, MTOR
TORC1 complex 1 MTOR
TORC2 complex 1 MTOR
Single-pass type I membrane protein 2 CD4, HLA-A
Secreted 3 BCHE, INS, SHBG
extracellular region 3 BCHE, INS, SHBG
Mitochondrion outer membrane 1 MTOR
Single-pass membrane protein 2 CYP2D6, HLA-A
mitochondrial outer membrane 2 MTOR, TSPO
anchoring junction 1 KCNA1
transcription regulator complex 1 NR1I2
external side of plasma membrane 2 CD4, HLA-A
T-tubule 2 SCN1A, SCN2A
perikaryon 1 KCNA1
Z disc 1 SCN1A
beta-catenin destruction complex 1 AXIN2
cytoplasmic vesicle 1 KCNA1
Early endosome 1 CD4
postsynaptic membrane 1 KCNA1
Apical cell membrane 2 ABCC2, ABCG2
Membrane raft 2 ABCG2, CD4
Nucleus, PML body 1 MTOR
PML body 1 MTOR
Cell projection, neuron projection 1 SCN9A
chromatin 1 NR1I2
phagocytic vesicle membrane 1 HLA-A
brush border membrane 1 ABCG2
blood microparticle 1 BCHE
nuclear envelope 1 MTOR
Recycling endosome membrane 1 HLA-A
Endomembrane system 1 MTOR
endosome lumen 1 INS
axon initial segment 2 KCNA1, SCN1A
Cell projection, dendrite 1 KCNA1
Presynaptic cell membrane 1 KCNA1
intermediate filament cytoskeleton 1 NR1I2
voltage-gated potassium channel complex 1 KCNA1
secretory granule lumen 1 INS
Golgi lumen 1 INS
endoplasmic reticulum lumen 3 BCHE, CD4, INS
axon terminus 2 KCNA1, SCN9A
voltage-gated calcium channel complex 1 CACNA1I
transport vesicle 1 INS
node of Ranvier 3 SCN1A, SCN2A, SCN9A
paranode region of axon 2 KCNA1, SCN2A
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
endoplasmic reticulum exit site 1 HLA-A
ER to Golgi transport vesicle membrane 1 HLA-A
nuclear envelope lumen 1 BCHE
calyx of Held 1 KCNA1
clathrin-coated endocytic vesicle membrane 1 CD4
external side of apical plasma membrane 1 ABCG2
lumenal side of endoplasmic reticulum membrane 1 HLA-A
MHC class I peptide loading complex 1 HLA-A
Cytoplasmic vesicle, phagosome 1 MTOR
voltage-gated sodium channel complex 3 SCN1A, SCN2A, SCN9A
Golgi medial cisterna 1 HLA-A
T cell receptor complex 1 CD4
MHC class I protein complex 1 HLA-A
MHC class II protein complex 1 HLA-A
juxtaparanode region of axon 1 KCNA1


文献列表

  • Elackiya Sithamparanathan, Katarzyna Kujawa-Roeleveld, Huub H M Rijnaarts, Nora B Sutton. Hydroponic materials improve organic micropollutant removal in vertical flow constructed wetlands treating wastewater. Chemosphere. 2024 Mar; 352(?):141388. doi: 10.1016/j.chemosphere.2024.141388. [PMID: 38346507]
  • Zijing Wu, Yang Liu, Rongfu Huang, Weixiong Huang. Mechanistic investigation of the electricity and gallic acid synergistically accelerated Fe(III)/Fe(II) cycle for the degradation of carbamazepine. Chemosphere. 2024 Feb; 349(?):140915. doi: 10.1016/j.chemosphere.2023.140915. [PMID: 38070611]
  • Aree Wanasuntronwong, Supassanan Kaewsrisung, Nisanat Lakkhanachatpan, Rittinarong Meepong, Tawepong Arayapisit, Mayuree Tantisira. Standardized Centella asiatica extract ECa 233 alleviates pain hypersensitivity by modulating P2X3 in trigeminal neuropathic pain. Journal of applied oral science : revista FOB. 2024; 32(?):e20230337. doi: 10.1590/1678-7757-2023-0337. [PMID: 38198371]
  • Xia Qian, Yuqing Deng, Na Zhong, Yuxuan Li, Junhua Wang, Jinhua Yan, Wei Liu, Jinglei Ye, Jingchao Liu, Guobei Xiao. Study on the reversal of epileptic drug resistance by tetramethylpyrazine in combination with carbamazepine through modulation of P-Glycoprotein expression in rat brain microvessel endothelial cell. Cellular and molecular biology (Noisy-le-Grand, France). 2023 Nov; 69(11):254-259. doi: 10.14715/cmb/2023.69.11.38. [PMID: 38015511]
  • Clément Baratange, Hugo Baali, Véronique Gaillet, Isabelle Bonnard, Laurence Delahaut, Jean-Charles Gaillard, Dominique Grandjean, Stéphanie Sayen, Andrea Gallorini, Nathalie Le Bris, David Renault, Florian Breider, Jean-Luc Loizeau, Jean Armengaud, Claudia Cosio. Bioaccumulation and molecular effects of carbamazepine and methylmercury co-exposure in males of Dreissena polymorpha. The Science of the total environment. 2023 Nov; 897(?):165379. doi: 10.1016/j.scitotenv.2023.165379. [PMID: 37423277]
  • Radka Kodešová, Helena Švecová, Aleš Klement, Miroslav Fér, Antonín Nikodem, Ganna Fedorova, Oleksandra Rieznyk, Martin Kočárek, Alina Sadchenko, Alica Chroňáková, Roman Grabic. Contamination of water, soil, and plants by micropollutants from reclaimed wastewater and sludge from a wastewater treatment plant. The Science of the total environment. 2023 Oct; 907(?):167965. doi: 10.1016/j.scitotenv.2023.167965. [PMID: 37866592]
  • Huiting Yang, Xiaohong Gu, Huihui Chen, Qingfei Zeng, Zhigang Mao, You Ge. Omics techniques reveal the toxicity mechanisms of three antiepileptic drugs to juvenile zebrafish (Danio rerio) brain and liver. Aquatic toxicology (Amsterdam, Netherlands). 2023 Sep; 262(?):106668. doi: 10.1016/j.aquatox.2023.106668. [PMID: 37659109]
  • Yishi Wang, Wei Qiu, Xiaohui Lu, Xiaoqun Zhou, Haochen Zhang, Xiuxue Gong, Baocai Gong, Jun Ma. Nitrilotriacetic acid-assisted Mn(II) activated periodate for rapid and long-lasting degradation of carbamazepine: The importance of Mn(IV)-oxo species. Water research. 2023 Aug; 241(?):120156. doi: 10.1016/j.watres.2023.120156. [PMID: 37270944]
  • Anna Mascellani, Filip Mercl, Sebnem Kurhan, Lorenzo Pierdona, Jiri Kudrna, Veronika Zemanova, Frantisek Hnilicka, Pavel Kloucek, Pavel Tlustos, Jaroslav Havlik. Biochemical and physiological changes in Zea mays L. after exposure to the environmental pharmaceutical pollutant carbamazepine. Chemosphere. 2023 Jul; 329(?):138689. doi: 10.1016/j.chemosphere.2023.138689. [PMID: 37059200]
  • Opeyemi Osuntokun, Gbola Olayiwola, Taiwo Adekemi Abayomi, Alimat Toyin Lawal, Opeyemi Samson Adeleke, Abiodun Oladele Ayoka. Mucuna pruriens seed repeals the hypothalamic-pituitary-testicular axis disruption following carbamazepine treatment in male Wistar rats. Nigerian journal of physiological sciences : official publication of the Physiological Society of Nigeria. 2023 Jun; 38(1):113-119. doi: 10.54548/njps.v38i1.16. [PMID: 38243374]
  • Débora Jesabel Pérez, Lucas Rodrigo Lombardero, William Joseph Doucette. Influence of exposure time, physicochemical properties, and plant transpiration on the uptake dynamics and translocation of pharmaceutical and personal care products in the aquatic macrophyte Typha latifolia. The Science of the total environment. 2023 Jun; ?(?):165107. doi: 10.1016/j.scitotenv.2023.165107. [PMID: 37364828]
  • Xin Yang, Jia-Yi He, Xiang-Xin Guo, Rong Tian. [Amino acid metabolism characteristics of Banxia Baizhu Tianma Decoction in realizing drug withdrawal based on transcriptomic analysis]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2023 May; 48(9):2512-2521. doi: 10.19540/j.cnki.cjcmm.20230117.702. [PMID: 37282880]
  • Jeong-In Hwang, P Chris Wilson. Absorption, translocation, and metabolism of atrazine, carbamazepine, and sulfamethoxazole by the macrophyte Orange King Humbert canna lily (Canna × generalis L.H. Bailey (pro sp.) [glauca × indica]). Environmental science and pollution research international. 2023 Jan; ?(?):. doi: 10.1007/s11356-023-25400-2. [PMID: 36719575]
  • Ashokkumar Sibiya, Jeyaraj Jeyavani, Manoharan Saravanan, Mohammed F Albeshr, Marcello Nicoletti, Marimuthu Govindarajan, Baskaralingam Vaseeharan. Response of hepatic biochemical parameters and neurotoxicity to carbamazepine and ibuprofen in Oreochromis mossambicus. Fish physiology and biochemistry. 2023 Jan; ?(?):. doi: 10.1007/s10695-023-01172-x. [PMID: 36717424]
  • Márton Pápai, Tibor Benedek, András Táncsics, Till L V Bornemann, Julia Plewka, Alexander J Probst, Daood Hussein, Gergely Maróti, Ofir Menashe, Balázs Kriszt. Selective enrichment, identification, and isolation of diclofenac, ibuprofen, and carbamazepine degrading bacteria from a groundwater biofilm. Environmental science and pollution research international. 2023 Jan; ?(?):. doi: 10.1007/s11356-022-24975-6. [PMID: 36690856]
  • Sanjeeb Mohapatra, Daniel Snow, Patrick Shea, Andy Gálvez-Rodríguez, Manish Kumar, Lokesh P Padhye, Suparna Mukherji. Photodegradation of a mixture of five pharmaceuticals commonly found in wastewater: Experimental and computational analysis. Environmental research. 2023 01; 216(Pt 3):114659. doi: 10.1016/j.envres.2022.114659. [PMID: 36328221]
  • L Ponce-Robles, L Benelhadj, A J García-García, F Pedrero-Salcedo, P A Nortes-Tortosa, J Albacete, J J Alarcón. Risk assessment for uptake and accumulation of pharmaceuticals by baby leaf lettuce irrigated with reclaimed water under commercial agricultural activities. Journal of environmental management. 2022 Dec; 324(?):116321. doi: 10.1016/j.jenvman.2022.116321. [PMID: 36179471]
  • Vasiliki G Beretsou, Maria-Christina Nika, Kyriakos Manoli, Costas Michael, Qian Sui, Lian Lundy, D Michael Revitt, Nikolaos S Thomaidis, Despo Fatta-Kassinos. Multiclass target analysis of contaminants of emerging concern including transformation products, soil bioavailability assessment and retrospective screening as tools to evaluate risks associated with reclaimed water reuse. The Science of the total environment. 2022 Dec; 852(?):158391. doi: 10.1016/j.scitotenv.2022.158391. [PMID: 36049679]
  • Patricia K Akao, Aviv Kaplan, Dror Avisar, Amit Dhir, Adi Avni, Hadas Mamane. Removal of carbamazepine, venlafaxine and iohexol from wastewater effluent using coupled microalgal-bacterial biofilm. Chemosphere. 2022 Dec; 308(Pt 2):136399. doi: 10.1016/j.chemosphere.2022.136399. [PMID: 36099989]
  • Manthiram Karthik Ravichandran, Ligy Philip. Fate of carbamazepine and its effect on physiological characteristics of wetland plant species in the hydroponic system. The Science of the total environment. 2022 Nov; 846(?):157337. doi: 10.1016/j.scitotenv.2022.157337. [PMID: 35842149]
  • Yuichi Tateishi, Nobutsune Ishikawa, Yoshiyuki Kobayashi, Hiroki Izumo, Yuta Eguchi, Satoshi Okada. Effect of Lacosamide therapy on blood cells and IgA levels in children and adolescents with epilepsy in a clinical setting. Epilepsy research. 2022 11; 187(?):107030. doi: 10.1016/j.eplepsyres.2022.107030. [PMID: 36308995]
  • Sijin He, Qigang Chen, Zhicong Jing, Lihua Gu, Kaixuan Luo. Avellis syndrome with ipsilateral prosopalgia, glossopharyngeal neuralgia, and central post-stroke pain: A case report and literature review. Medicine. 2022 Sep; 101(39):e30669. doi: 10.1097/md.0000000000030669. [PMID: 36181064]
  • Shan Zhou, Ruitong Li, Ziyi Chen, Ruina Ren, Xueding Wang, Qilin Dai, Dingshen Wen, Yanping Guan, Xiaoxu Zhang, Siyuan Tang, Liemin Zhou, Min Huang. LC-MS/MS quantification of levetiracetam, lamotrigine and 10-hydroxycarbazepine in TDM of epileptic patients. Biomedical chromatography : BMC. 2022 Aug; 36(8):e5393. doi: 10.1002/bmc.5393. [PMID: 35527473]
  • Tingting Wu, Huan Peng, Xiaowei Liu, Ruijin Wu. Removal of Carbamazepine in Aqueous Solution by CoS2/Fe2+/PMS Process. Molecules (Basel, Switzerland). 2022 Jul; 27(14):. doi: 10.3390/molecules27144524. [PMID: 35889397]
  • Lin Wu, Yasong Li, Xiangke Kong, Xiaohua Zhu. Mechanism evolution and prediction of carbamazepine sorption by mangrove plant residue-derived biochars. Journal of environmental quality. 2022 Jul; 51(4):745-754. doi: 10.1002/jeq2.20359. [PMID: 35460589]
  • Fatma Ilgaz, Selin Seda Timur, Cemil Can Eylem, Emirhan Nemutlu, Çiğdem Eroğlu Erdem, Hakan Eroğlu, Hülya Gökmen-Özel. Do Thickening Agents Used in Dysphagia Diet Affect Drug Bioavailability?. European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences. 2022 Jul; 174(?):106197. doi: 10.1016/j.ejps.2022.106197. [PMID: 35489612]
  • Ivana Kacirova, Milan Grundmann, Hana Brozmanova. Carbamazepine and carbamazepine-epoxide concentrations in mothers, colostrum, and breastfed newborns: Comparison with concentrations determined during delivery and in the mature milk period. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. 2022 Jul; 151(?):113176. doi: 10.1016/j.biopha.2022.113176. [PMID: 35623166]
  • Tibor Benedek, Márton Pápai, Kholood Gharieb, Anna Bedics, András Táncsics, Erika Tóth, Hussein Daood, Gergely Maróti, Roland Wirth, Ofir Menashe, Károly Bóka, Balázs Kriszt. Nocardioides carbamazepini sp. nov., an ibuprofen degrader isolated from a biofilm bacterial community enriched on carbamazepine. Systematic and applied microbiology. 2022 Jul; 45(4):126339. doi: 10.1016/j.syapm.2022.126339. [PMID: 35714383]
  • Hong Yao, Xu Zhang, Fang Liu, Shaobin Sun. Removal of carbamazepine (CBZ) from synthetic urine by FeOCl-coated ceramic membrane: The study of kinetic modeling. Chemosphere. 2022 Jul; 298(?):134222. doi: 10.1016/j.chemosphere.2022.134222. [PMID: 35259365]
  • Arzu Ulvi, Senar Aydın, Mehmet Emin Aydın. Fate of selected pharmaceuticals in hospital and municipal wastewater effluent: occurrence, removal, and environmental risk assessment. Environmental science and pollution research international. 2022 Jun; ?(?):. doi: 10.1007/s11356-022-21131-y. [PMID: 35655023]
  • Meiyun Shi, Xinyue Zheng, Di Lu, Xujian Duan, Yongqi Wang, Yajun Liu, Hongyu Xue, Lei Yin. Ultrafast and high-throughput quantitative analysis of carbamazepine in human plasma by direct analysis in real time tandem mass spectrometry coupled with solid phase extraction to eliminate matrix effects. Journal of pharmaceutical and biomedical analysis. 2022 May; 214(?):114751. doi: 10.1016/j.jpba.2022.114751. [PMID: 35398614]
  • Rajeshwar Kamal Kant Arya, Vijay Juyal, Dheeraj Bisht, Mohammad Rashid, Abdulmalik Saleh Alfawaz Altamimi, Obaid Afzal, Neeraj Kumar Sethiya. Enhanced Brain Delivery via Intranasal Administration of Carbamazepine Loaded Solid Lipid Nanoparticles: Optimization, Pharmacokinetic analysis, In-vitro and In-vivo Drug Release Study. Current drug delivery. 2022 05; ?(?):. doi: 10.2174/1567201819666220519120837. [PMID: 35598246]
  • Dawood Aghamohammadi, Shahrzad Sharifi, Seyed Kazem Shakouri, Yashar Eslampour, Neda Dolatkhah. Autologous conditioned serum (Orthokine) injection for treatment of classical trigeminal neuralgia: results of a single-center case series. Journal of medical case reports. 2022 May; 16(1):183. doi: 10.1186/s13256-022-03393-9. [PMID: 35526052]
  • Alessandro Nardi, Marica Mezzelani, Silvana Costa, Giuseppe d'Errico, Maura Benedetti, Stefania Gorbi, Rosa Freitas, Francesco Regoli. Marine heatwaves hamper neuro-immune and oxidative tolerance toward carbamazepine in Mytilus galloprovincialis. Environmental pollution (Barking, Essex : 1987). 2022 May; 300(?):118970. doi: 10.1016/j.envpol.2022.118970. [PMID: 35143899]
  • Jose de Leon. Precision psychiatry: The complexity of personalizing antipsychotic dosing. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology. 2022 05; 58(?):80-85. doi: 10.1016/j.euroneuro.2022.03.001. [PMID: 35314415]
  • Mehmet Bulbul, Bilge Aydın Turk, Talip Karaçor, Muhittin Onderci, Mehmet Can Nacar, Ali Parlar, Cihat Ucar. Carbamazepine protects the endometrium against negative effects of estrogen in rats. Biotechnic & histochemistry : official publication of the Biological Stain Commission. 2022 May; 97(4):254-260. doi: 10.1080/10520295.2021.1942988. [PMID: 34162294]
  • Zhaorui Song, Xinhui Zhai, Chenrui Jiang, Rong Chen, Sijing Ye, Jinzhe Tong, Pierre Dramou, Hua He. Sensitive and selective detection of carbamazepine in serum samples by bionic double-antibody sandwich method based on cucurbit[7]uril and molecular imprinted polymers. Biosensors & bioelectronics. 2022 May; 203(?):114037. doi: 10.1016/j.bios.2022.114037. [PMID: 35123315]
  • Ching-Han Lin, Yu-Chi Lin, Shi-Bing Yang, Pei-Chun Chen. Carbamazepine promotes surface expression of mutant Kir6.2-A28V ATP-sensitive potassium channels by modulating Golgi retention and autophagy. The Journal of biological chemistry. 2022 05; 298(5):101904. doi: 10.1016/j.jbc.2022.101904. [PMID: 35398096]
  • Clément Baratange, Séverine Paris-Palacios, Isabelle Bonnard, Laurence Delahaut, Dominique Grandjean, Laurence Wortham, Stéphanie Sayen, Andrea Gallorini, Jean Michel, David Renault, Florian Breider, Jean-Luc Loizeau, Claudia Cosio. Metabolic, cellular and defense responses to single and co-exposure to carbamazepine and methylmercury in Dreissena polymorpha. Environmental pollution (Barking, Essex : 1987). 2022 May; 300(?):118933. doi: 10.1016/j.envpol.2022.118933. [PMID: 35122922]
  • Julija Čiauškaitė, Giedrė Gelžinienė, Giedrė Jurkevičienė. Oxcarbazepine and Hyponatremia. Medicina (Kaunas, Lithuania). 2022 Apr; 58(5):. doi: 10.3390/medicina58050559. [PMID: 35629976]
  • K Nagai, S Fukuno, R Moriwaki, H Kuroda, S Omotani, T Miura, Y Hatsuda, M Myotoku, H Konishi. Influence of concurrent and staggered dosing of semi-solid nutrients on the pharmacokinetics of orally administered carbamazepine in rats. Die Pharmazie. 2022 04; 77(3):118-120. doi: 10.1691/2022.1756. [PMID: 35459440]
  • Claudia Cristina Ferreira Vasconcelos, Mariana Beiral Hammerle, Deborah Santos Sales, Fernanda Cristina Rueda Lopes, Patricia Gomes Pinheiro, Elisa Gutman Gouvea, Manuella Caroline Dutra Frazão Alves, Tayane Vasconcellos Pereira, Sergio Luis Schmidt, Regina Maria Papais Alvarenga, Karina Lebeis Pires. Post-COVID-19 olfactory dysfunction: carbamazepine as a treatment option in a series of cases. Journal of neurovirology. 2022 04; 28(2):312-318. doi: 10.1007/s13365-022-01066-3. [PMID: 35366736]
  • Yannick Lipecki, Ekkehard Haen. Simultaneous Quantification of 11 Antiseizure Medications and Metabolites in Serum for Therapeutic Drug Monitoring Using High-Performance Liquid Chromatography with Ultraviolet Detection: A Short Communication. Therapeutic drug monitoring. 2022 04; 44(2):345-350. doi: 10.1097/ftd.0000000000000908. [PMID: 35292610]
  • Page B Pennell, Ashwin Karanam, Kimford J Meador, Elizabeth Gerard, Laura Kalayjian, Patricia Penovich, Abigail Matthews, Thomas M McElrath, Angela K Birnbaum. Antiseizure Medication Concentrations During Pregnancy: Results From the Maternal Outcomes and Neurodevelopmental Effects of Antiepileptic Drugs (MONEAD) Study. JAMA neurology. 2022 04; 79(4):370-379. doi: 10.1001/jamaneurol.2021.5487. [PMID: 35157004]
  • Naga Chalasani, Herbert L Bonkovsky, Jonathan G Stine, Jiezhun Gu, Huiman Barnhart, Elin Jacobsen, Einar Björnsson, Robert J Fontana, David E Kleiner, Jay H Hoofnagle. Clinical characteristics of antiepileptic-induced liver injury in patients from the DILIN prospective study. Journal of hepatology. 2022 Apr; 76(4):832-840. doi: 10.1016/j.jhep.2021.12.013. [PMID: 34953957]
  • Giulia Liparoti, Beatrice Burchiani, Elisabetta Mencaroni, Domenico Tripodi, Giuseppe Di Cara, Alberto Verrotti. Individualizing doses of antiepileptic drugs. Expert opinion on drug metabolism & toxicology. 2022 Mar; 18(3):219-233. doi: 10.1080/17425255.2022.2075342. [PMID: 35523739]
  • Jia Chen, Lihua Bai, Yani He. A possible case of carbamazepine-induced renal phospholipidosis mimicking Fabry disease. Clinical and experimental nephrology. 2022 Mar; 26(3):303-304. doi: 10.1007/s10157-021-02172-y. [PMID: 35059891]
  • Weixuan Zhao, Hongmei Meng. Effects of genetic polymorphism of drug-metabolizing enzymes on the plasma concentrations of antiepileptic drugs in Chinese population. Bioengineered. 2022 03; 13(3):7709-7745. doi: 10.1080/21655979.2022.2036916. [PMID: 35290166]
  • Min-Hui Tan, Seow-Yeing Yee, Rosnawati Yahya. Lessons of the month 2: A case of inappropriate drug-drug interaction in kidney transplant. Clinical medicine (London, England). 2022 03; 22(2):169-171. doi: 10.7861/clinmed.2021-0789. [PMID: 35304379]
  • Ken-Ichi Oba, Hiroaki Shimada, Ryota Hashimoto, Atsushi Kawase, Takeo Nakanishi, Masahiro Iwaki. Assessment of hepatic prostaglandin E2 level in carbamazepine induced liver injury. Endocrine regulations. 2022 Feb; 56(1):22-30. doi: 10.2478/enr-2022-0003. [PMID: 35180822]
  • Takahiro Kanai, Takane Ito, Jun Aoyagi, Takanori Yamagata. Membranous nephropathy without vacuolated podocytes in Fabry disease treated with agalsidase-β and carbamazepine: A case report. Medicine. 2022 Feb; 101(7):e28830. doi: 10.1097/md.0000000000028830. [PMID: 35363176]
  • Dongxiao Ma, Zhengchao Ji, Haiwei Cao, Jing Huang, Lei Zeng, Lei Yin. LC-MS3 Strategy for Quantification of Carbamazepine in Human Plasma and Its Application in Therapeutic Drug Monitoring. Molecules (Basel, Switzerland). 2022 Feb; 27(4):. doi: 10.3390/molecules27041224. [PMID: 35209012]
  • Jing Wang, Chong Li, Peng Li. A Small Footprint and Robust Interface for Solid Phase Microextraction and Mass Spectrometry Based on Vibrating Sharp-Edge Spray Ionization. Journal of the American Society for Mass Spectrometry. 2022 Feb; 33(2):304-314. doi: 10.1021/jasms.1c00305. [PMID: 35040644]
  • Yoko Urashima, Honami Kobayashi, Kana Yamamoto, Kazuki Matsushita, Kazuya Urashima, Masahiko Tsujikawa, Kaoru Suzuki, Kazumi Kurachi, Masami Nishihara, Masashi Neo, Michiaki Myotoku, Takuro Kobori, Tokio Obata. Liquid Enteral Nutrients Alter the Pharmacokinetics of Orally Administered Carbamazepine in Rats. International journal of medical sciences. 2022; 19(5):789-795. doi: 10.7150/ijms.71770. [PMID: 35693745]
  • Thibaut Dumas, Frédérique Courant, Christine Almunia, Julien Boccard, David Rosain, Geoffroy Duporté, Jean Armengaud, Hélène Fenet, Elena Gomez. An integrated metabolomics and proteogenomics approach reveals molecular alterations following carbamazepine exposure in the male mussel Mytilus galloprovincialis. Chemosphere. 2022 Jan; 286(Pt 2):131793. doi: 10.1016/j.chemosphere.2021.131793. [PMID: 34364230]
  • Ryo Ichikawa, Sosuke Masuda, Junta Nakahara, Mio Kobayashi, Risako Yamashita, Suzuka Uomoto, Ohshima Kanami, Erika Hara, Yuko Ito, Makoto Shibutani, Toshinori Yoshida. Inhibition of autophagy with expression of NADPH oxidase subunit p22phox in preneoplastic lesions in a high-fat diet and streptozotocin-related hepatocarcinogenesis rat model. The Journal of toxicological sciences. 2022; 47(7):289-300. doi: 10.2131/jts.47.289. [PMID: 35786680]
  • Ke-Yu Chen, Ruo-Yang Li. Efficacy and safety of different antidepressants and anticonvulsants in central poststroke pain: A network meta-analysis and systematic review. PloS one. 2022; 17(10):e0276012. doi: 10.1371/journal.pone.0276012. [PMID: 36227855]
  • Ming-Liang Zhang, Xiao-Long Chen, Zhao-Fang Bai, Xu Zhao, Wei-Xia Li, Xiao-Yan Wang, Hui Zhang, Xiao-Fei Chen, Shu-Qi Zhang, Jin-Fa Tang, Xiao-He Xiao, Yan-Ling Zhao. ABCB1 c.3435C > T and EPHX1 c.416A > G polymorphisms influence plasma carbamazepine concentration, metabolism, and pharmacoresistance in epileptic patients. Gene. 2021 Dec; 805(?):145907. doi: 10.1016/j.gene.2021.145907. [PMID: 34411648]
  • Priyamvada Sharma, David Hanigan. Evidence of low levels of trace organic contaminants in terminal lakes. Chemosphere. 2021 Dec; 285(?):131408. doi: 10.1016/j.chemosphere.2021.131408. [PMID: 34242983]
  • Fatma Şimşek, Mustafa Ceylan, Ahmet Kızıltunç, İbrahim İyigün. The correlation between carbamazepine and valproic acid monotherapy with serum adiponectin and carnitine. Acta neurologica Belgica. 2021 Dec; 121(6):1823-1830. doi: 10.1007/s13760-020-01552-7. [PMID: 33242193]
  • Zhen-E Xu, Wei-Bin Li, Meng-Yuan Qiao, Hong-Tao Cui, Ling-Zhi Zhao, Qi-Xiong Chen, Jing-Kun Miao. Comparative efficacy of anti-epileptic drugs for neonatal seizures: A network meta-analysis. Pediatrics and neonatology. 2021 11; 62(6):598-605. doi: 10.1016/j.pedneo.2021.06.005. [PMID: 34389261]
  • Tianlang Zhang, Nan Li, Guosheng Chen, Jianqiao Xu, Gangfeng Ouyang, Fang Zhu. Stress symptoms and plant hormone-modulated defense response induced by the uptake of carbamazepine and ibuprofen in Malabar spinach (Basella alba L.). The Science of the total environment. 2021 Nov; 793(?):148628. doi: 10.1016/j.scitotenv.2021.148628. [PMID: 34328997]
  • Luca Ricciardi, Michele Acqui, Resi Pucci, Christian Napoli, Alba Scerrati. Transient Trigeminal Neuralgia Recurrence During Coronavirus disease-19 in Carbamazepine Responders Patients. The Journal of craniofacial surgery. 2021 Nov; 32(8):e834. doi: 10.1097/scs.0000000000007893. [PMID: 34292248]
  • Duygu Eryavuz Onmaz, Sedat Abusoglu, Bahadir Ozturk, Gulsum Abusoglu, Fatma Humeyra Yerlikaya, Ali Unlu. Determination of serum carbamazepine and its metabolite by validated tandem mass spectrometric method and the effect of carbamazepine on various hematological and biochemical parameters. Journal of pharmaceutical and biomedical analysis. 2021 Oct; 205(?):114299. doi: 10.1016/j.jpba.2021.114299. [PMID: 34388672]
  • Dawa Droma, Saurav Kumar, Tapas Paul, Prasenjit Pal, Neelam Saharan, Kundan Kumar, Nalini Poojary. Biomarkers for assessing chronic toxicity of carbamazepine, an anticonvulsants drug on Pangasianodon hypophthalmus (Sauvage, 1878). Environmental toxicology and pharmacology. 2021 Oct; 87(?):103691. doi: 10.1016/j.etap.2021.103691. [PMID: 34153508]
  • Ingrid Fricke-Galindo, Helgi Jung-Cook, Iris E Martínez-Juárez, Nancy Monroy-Jaramillo, Alberto Ortega-Vázquez, Irma S Rojas-Tomé, Pedro Dorado, Eva Peñas-Lledó, Adrián Llerena, Marisol López-López. Relevance of NR1I2 variants on carbamazepine therapy in Mexican Mestizos with epilepsy at a tertiary-care hospital. Pharmacogenomics. 2021 10; 22(15):983-996. doi: 10.2217/pgs-2021-0081. [PMID: 34612084]
  • Adaobi I Bisi-Onyemaechi, Ugo N Chikani, Ndubuisi A Uwaezuoke, Ann E Aronu, Ngozi C Ojinnaka. Serum folate levels in children on long-term anti-seizure medication in a Nigerian tertiary center-Implications for practice and public health. Science progress. 2021 Oct; 104(4):368504211057680. doi: 10.1177/00368504211057680. [PMID: 34816782]
  • Hanieh Kefayati, Yadollah Yamini, Maryam Shamsayei, Siamak Abdi. Molecularly imprinted polypyrrole@CuO nanocomposite as an in-tube solid-phase microextraction coating for selective extraction of carbamazepine from biological samples. Journal of pharmaceutical and biomedical analysis. 2021 Sep; 204(?):114256. doi: 10.1016/j.jpba.2021.114256. [PMID: 34280818]
  • Marta Karaźniewicz-Łada, Anna K Główka, Aniceta A Mikulska, Franciszek K Główka. Pharmacokinetic Drug-Drug Interactions among Antiepileptic Drugs, Including CBD, Drugs Used to Treat COVID-19 and Nutrients. International journal of molecular sciences. 2021 Sep; 22(17):. doi: 10.3390/ijms22179582. [PMID: 34502487]
  • Inês Leitão, Miguel Pedro Mourato, Luísa Carvalho, Maria Conceição Oliveira, Maria Matilde Marques, Luisa Louro Martins. Antioxidative response of lettuce (Lactuca sativa) to carbamazepine-induced stress. Environmental science and pollution research international. 2021 Sep; 28(33):45920-45932. doi: 10.1007/s11356-021-13979-3. [PMID: 33881698]
  • Ana Ferreira, Márcio Rodrigues, Sara Meirinho, Ana Fortuna, Amílcar Falcão, Gilberto Alves. Silymarin as a flavonoid-type P-glycoprotein inhibitor with impact on the pharmacokinetics of carbamazepine, oxcarbazepine and phenytoin in rats. Drug and chemical toxicology. 2021 Sep; 44(5):458-469. doi: 10.1080/01480545.2019.1601736. [PMID: 31020859]
  • Ting Hu, Xiaoxi Zeng, Tian Tian, Jinping Liu. Association of EPHX1 polymorphisms with plasma concentration of carbamazepine in epileptic patients: Systematic review and meta-analysis. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia. 2021 Sep; 91(?):159-171. doi: 10.1016/j.jocn.2021.07.009. [PMID: 34373022]
  • Mengmeng Zheng, Chunpu Li, Mi Zhou, Ru Jia, Gang Cai, Fengyu She, Lulu Wei, Shaohui Wang, Jie Yu, Dingyan Wang, Laurent Calcul, Xingmin Sun, Xiaomin Luo, Feng Cheng, Qi Li, Yan Wang, Jianfeng Cai. Discovery of Cyclic Peptidomimetic Ligands Targeting the Extracellular Domain of EGFR. Journal of medicinal chemistry. 2021 08; 64(15):11219-11228. doi: 10.1021/acs.jmedchem.1c00607. [PMID: 34297567]
  • Orlando Salinas-Jaramillo, Alejandra Monroy-Arreola, Sebastian Herrera-Noreña, Ana L Guzmán-Ortiz, Abrahan Hernández-Hernández, Silvia Méndez-Flores, Judith Domínguez-Cherit, Noe V Duran-Figueroa, Dean J Naisbitt, Pedro Cortes-Reynosa, Eduardo Perez Salazar, Héctor Quezada, J Luis Castrejón-Flores. Extracellular Vesicles from Human Plasma Show a Distinctive Proteome and miRNome Profile in Patients with Severe Cutaneous Adverse Reactions. Chemical research in toxicology. 2021 07; 34(7):1738-1748. doi: 10.1021/acs.chemrestox.1c00047. [PMID: 34142820]
  • Gui-Xin Zhao, Zheng Zhang, Wen-Ke Cai, Ming-Li Shen, Ping Wang, Gong-Hao He. Associations between CYP3A4, CYP3A5 and SCN1A polymorphisms and carbamazepine metabolism in epilepsy: A meta-analysis. Epilepsy research. 2021 07; 173(?):106615. doi: 10.1016/j.eplepsyres.2021.106615. [PMID: 33756436]
  • Daniel W Griepp, David J Kim, Marc Ganz, Eugene J Dolphin, Nadia Sotudeh, Steven A Burekhovich, Qais Naziri. The effects of antiepileptic drugs on bone health: A systematic review. Epilepsy research. 2021 Jul; 173(?):106619. doi: 10.1016/j.eplepsyres.2021.106619. [PMID: 33774428]
  • Eulalia María Beltrán, Carlos Fernández-Torija, María Victoria Pablos, Miguel Ángel Porcel, Pilar García-Hortigüela, Miguel González-Doncel. The effect of PFOs on the uptake and translocation of emerging contaminants by crops cultivated under soil and soilless conditions. Ecotoxicology and environmental safety. 2021 Jun; 215(?):112103. doi: 10.1016/j.ecoenv.2021.112103. [PMID: 33740485]
  • Zhonghui Bai, Kun Jia, Guilan Chen, Xinjun Liao, Zigang Cao, Yangqi Zhao, Chunping Zhang, Huiqiang Lu. Carbamazepine induces hepatotoxicity in zebrafish by inhibition of the Wnt/β-catenin signaling pathway. Environmental pollution (Barking, Essex : 1987). 2021 May; 276(?):116688. doi: 10.1016/j.envpol.2021.116688. [PMID: 33611196]
  • Sua Kim, Chor Ho Jo, Gheun-Ho Kim. Psychotropic drugs upregulate aquaporin-2 via vasopressin-2 receptor/cAMP/protein kinase A signaling in inner medullary collecting duct cells. American journal of physiology. Renal physiology. 2021 05; 320(5):F963-F971. doi: 10.1152/ajprenal.00576.2020. [PMID: 33843270]
  • Ivana Kacirova, Milan Grundmann, Hana Brozmanova. Therapeutic monitoring of carbamazepine and its active metabolite during the 1st postnatal month: Influence of drug interactions. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. 2021 May; 137(?):111412. doi: 10.1016/j.biopha.2021.111412. [PMID: 33761618]
  • R M Müller, B Herziger, S Jeschke, M P Neininger, T Bertsche, A Bertsche. Knowledge of epilepsy among German pharmacists. Epilepsy research. 2021 05; 172(?):106587. doi: 10.1016/j.eplepsyres.2021.106587. [PMID: 33647738]
  • Mauricio A García, Rodrigo Cristofoletti, Bertil Abrahamsson, Dirk W Groot, Alan Parr, James E Polli, Mehul Mehta, Vinod P Shah, Tajiri Tomakazu, Jennifer B Dressman, Peter Langguth. Biowaiver Monograph for Immediate-Release Solid Oral Dosage Forms: Carbamazepine. Journal of pharmaceutical sciences. 2021 05; 110(5):1935-1947. doi: 10.1016/j.xphs.2021.02.019. [PMID: 33610571]
  • Mark J Henderson, Kathleen A Trychta, Shyh-Ming Yang, Susanne Bäck, Adam Yasgar, Emily S Wires, Carina Danchik, Xiaokang Yan, Hideaki Yano, Lei Shi, Kuo-Jen Wu, Amy Q Wang, Dingyin Tao, Gergely Zahoránszky-Kőhalmi, Xin Hu, Xin Xu, David Maloney, Alexey V Zakharov, Ganesha Rai, Fumihiko Urano, Mikko Airavaara, Oksana Gavrilova, Ajit Jadhav, Yun Wang, Anton Simeonov, Brandon K Harvey. A target-agnostic screen identifies approved drugs to stabilize the endoplasmic reticulum-resident proteome. Cell reports. 2021 04; 35(4):109040. doi: 10.1016/j.celrep.2021.109040. [PMID: 33910017]
  • Andreia Carona, Joana Bicker, Rui Silva, Ana Silva, Isabel Santana, Francisco Sales, Amílcar Falcão, Ana Fortuna. HPLC method for the determination of antiepileptic drugs in human saliva and its application in therapeutic drug monitoring. Journal of pharmaceutical and biomedical analysis. 2021 Apr; 197(?):113961. doi: 10.1016/j.jpba.2021.113961. [PMID: 33626445]
  • Cristóbal Espinosa-Ruiz, Simona Manuguerra, Maria Morghese, José María García-Beltrán, María Ángeles Esteban, Marta Giuga, Concetta M Messina, Andrea Santulli. Immunity and inflammatory responses in gilthead sea bream (Sparus aurata L.) exposed to sub-lethal mixture of carbamazepine, cadmium chloride and polybrominated diphenyl ether. Fish & shellfish immunology. 2021 Apr; 111(?):25-35. doi: 10.1016/j.fsi.2020.12.013. [PMID: 33359412]
  • Anke Zhang, Wenbo Zhang, Houshi Xu, Chenqi Guo, Ling Yuan, Yuanzhi Xu, Jie Ren, Lingzhao Min, Qiuyang Sun, Meiqing Lou, Lili Wei, Shaojian Lin. Diabetes mellitus contributes to carbamazepine resistance in patient with trigeminal neuralgia. Neurosurgical review. 2021 Apr; 44(2):1119-1125. doi: 10.1007/s10143-020-01304-4. [PMID: 32333283]
  • Prateek Kumar Panda, Indar Kumar Sharawat. Impact of carbamazepine and lacosamide on serum lipid levels. Epilepsia. 2021 04; 62(4):1034-1035. doi: 10.1111/epi.16859. [PMID: 33651399]
  • Samara U Oliva, Rhaiza R Andretta, Joana N Simas, Renato B Tesser, Camila C Paccola, Sandra M Miraglia. Thyroid hormones, Sertoli cell proliferation and differentiation in progenies from carbamazepine-treated rat dams during pregnancy and lactation. Andrologia. 2021 Apr; 53(3):e13969. doi: 10.1111/and.13969. [PMID: 33433934]
  • Yoonhyuk Jang, Seonghae Yoon, Tae-Joon Kim, SeungHwan Lee, Kyung-Sang Yu, In-Jin Jang, Kon Chu, Sang Kun Lee. Population pharmacokinetic model development and its relationship with adverse events of oxcarbazepine in adult patients with epilepsy. Scientific reports. 2021 03; 11(1):6370. doi: 10.1038/s41598-021-85920-0. [PMID: 33737678]
  • Kai Huang, Linling Que, Ying Ding, Nannan Chu, Zhenzhong Qian, Wei Qin, Yuanxing Chen, Jisheng Zhang, Qing He. Identification of human uridine diphosphate-glucuronosyltransferase isoforms responsible for the glucuronidation of 10,11-dihydro-10-hydroxy-carbazepine. The Journal of pharmacy and pharmacology. 2021 Mar; 73(3):388-397. doi: 10.1093/jpp/rgaa059. [PMID: 33793880]
  • Giuseppe Brunetti, Radka Kodešová, Helena Švecová, Miroslav Fér, Antonín Nikodem, Aleš Klement, Roman Grabic, Jiří Šimůnek. On the Use of Mechanistic Soil-Plant Uptake Models: A Comprehensive Experimental and Numerical Analysis on the Translocation of Carbamazepine in Green Pea Plants. Environmental science & technology. 2021 Mar; 55(5):2991-3000. doi: 10.1021/acs.est.0c07420. [PMID: 33587851]
  • Jeong-In Hwang, Francisca Ordonez Hinz, Joseph P Albano, Patrick Christopher Wilson. Enhanced dissipation of trace level organic contaminants by floating treatment wetlands established with two macrophyte species: A mesocosm study. Chemosphere. 2021 Mar; 267(?):129159. doi: 10.1016/j.chemosphere.2020.129159. [PMID: 33321276]
  • Isaac A Adedara, Babajide O Ajayi, Blessing A Afolabi, Ifeoluwa O Awogbindin, Joao B T Rocha, Ebenezer O Farombi. Toxicological outcome of exposure to psychoactive drugs carbamazepine and diazepam on non-target insect Nauphoeta cinerea. Chemosphere. 2021 Feb; 264(Pt 1):128449. doi: 10.1016/j.chemosphere.2020.128449. [PMID: 33032224]
  • Jiajing Xin, Saihong Yan, Xiangsheng Hong, Huan Zhang, Jinmiao Zha. Environmentally relevant concentrations of carbamazepine induced lipid metabolism disorder of Chinese rare minnow (Gobiocypris rarus) in a gender-specific pattern. Chemosphere. 2021 Feb; 265(?):129080. doi: 10.1016/j.chemosphere.2020.129080. [PMID: 33261836]
  • Ruotian Zhang, Min Yang, Yang Li, Hedong Liu, Maoxian Ren, Zhou-Shan Tao. Effect of alendronate on the femoral metaphyseal defect under carbamazepine in ovariectomized rats. Journal of orthopaedic surgery and research. 2021 Jan; 16(1):14. doi: 10.1186/s13018-020-02151-1. [PMID: 33407695]
  • Vicky M Pham, Jennifer M White, Steven R Gunther, Jonathan T Stewart. Lithium for Carbamazepine-Induced Syndrome of Inappropriate Antidiuretic Hormone. Clinical neuropharmacology. 2021 Jan; 44(1):33-34. doi: 10.1097/wnf.0000000000000421. [PMID: 33201007]
  • Huihui Chen, Xiaohong Gu, Qingfei Zeng, Zhigang Mao, Christopher J Martyniuk. Characterization of the GABAergic system in Asian clam Corbicula fluminea: Phylogenetic analysis, tissue distribution, and response to the aquatic contaminant carbamazepine. Comparative biochemistry and physiology. Toxicology & pharmacology : CBP. 2021 Jan; 239(?):108896. doi: 10.1016/j.cbpc.2020.108896. [PMID: 32949817]
  • Emna Gaies, Fatma Zgolli, Rim Charfi, Mouna Ben Sassi, Hanene El Jebari, Issam Salouage, Riadh Daghfous, Sameh Trabelsi. Drug interaction between carbamazepine and other antiepileptic drugs in Tunisian epileptic patients. La Tunisie medicale. 2021 Aou; 99(8):877-880. doi: NULL. [PMID: 35261014]
  • Marica Mezzelani, Alessandro Nardi, Ilaria Bernardini, Massimo Milan, Luca Peruzza, Giuseppe d'Errico, Daniele Fattorini, Stefania Gorbi, Tomaso Patarnello, Francesco Regoli. Environmental pharmaceuticals and climate change: The case study of carbamazepine in M. galloprovincialis under ocean acidification scenario. Environment international. 2021 01; 146(?):106269. doi: 10.1016/j.envint.2020.106269. [PMID: 33248345]