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1

Lech, Anna, Patrycja Garbacz, Artur Sikorski, Maria Gazda, and Marek Wesolowski. "New Saccharin Salt of Chlordiazepoxide: Structural and Physicochemical Examination." International Journal of Molecular Sciences 23, no. 19 (2022): 12050. http://dx.doi.org/10.3390/ijms231912050.

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Since the formation of organic salts can improve the solubility, bioavailability, and stability of active pharmaceutical ingredients, the aim of this work was to prepare an organic salt of chlordiazepoxide with saccharin. To achieve this goal, the saccharin salt of chlordiazepoxide was obtained from a physical mixture of both components by grinding them with a small volume of solvent and by crystallizing them with complete evaporation of the solvent. The resulting salt was examined by methods such as Powder X-ray Diffraction (PXRD), Single Crystal X-ray Diffraction (SCXRD), Differential Scanni
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2

Nokhodchi, Ali, Roya Talari, Hadi Valizadeh, and Mohammad Barzegar Jalali. "An investigation on the solid dispersions of chlordiazepoxide." International Journal of Biomedical Science 3, no. 3 (2007): 210–16. http://dx.doi.org/10.59566/ijbs.2007.3210.

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The aim of this study was to prepare solid dispersions of chlordiazepoxide techniques to improve its dissolution rate. To this end, three techniques namely, two solvent methods and co-grinding technique were used. Solid dispersions of chlordiazepoxide in polyvinylpyrrolidone (PVP), Eudragit E100, Mannitol and Sorbitol with two different ratios of drug to carrier (5:5 and 1:9) were prepared. These solid dispersions were evaluated using dissolution tester to monitor dissolution behaviour and Fourier-transform infrared spectroscopy to investigate interaction between the drug and carriers in solid
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3

Harvey, S. "Benzodiazepine antagonism of thyrotrophin-releasing hormone receptors: biphasic actions on growth hormone secretion in domestic fowl." Journal of Endocrinology 137, no. 1 (1993): 35–42. http://dx.doi.org/10.1677/joe.0.1370035.

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ABSTRACT Benzodiazepines are pharmacological agents widely used for their anxiolytic and anticonvulsant properties. However, as these drugs are known to antagonize the binding and action of thyrotrophin-releasing hormone (TRH) in pituitary tissue, the possibility that they may modulate GH secretion was investigated in domestic fowl, in which TRH is a GH-releasing factor. Chlordiazepoxide (an antagonist of central-type benzodiazepine receptors) had no significant effect on the basal release of GH from incubated chicken pituitary glands, but at concentrations > 10 μmol/l chlordiazepoxide supp
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4

Balston, Alfred, Kuljit Hunjan, and Michael J. Kelleher. "The use of chlordiazepoxide for outpatient gamma-butyrolactone (GBL) detoxification: An observational study." Drug Science, Policy and Law 9 (January 2023): 205032452311675. http://dx.doi.org/10.1177/20503245231167544.

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Background Various detoxification regimens are used for gamma-hydroxybutyrate (GHB) and gamma-butyrolactone (GBL), including diazepam, barbiturates, baclofen and GHB itself. However, these regimens are primarily derived from inpatient units, and literature on outpatient GBL detoxification is sparse with no previous reports on chlordiazepoxide. We describe the characteristics of outpatient GBL detoxification using chlordiazepoxide. Methods Observational study of all patients who attended a community outpatient addiction service in South London between August 2015 and November 2017 seeking detox
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5

&NA;. "Chlordiazepoxide withdrawal." Reactions Weekly &NA;, no. 647 (1997): 7. http://dx.doi.org/10.2165/00128415-199706470-00017.

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6

Hoey, Lori L., Avi Nahum, and Kyle Vance‐Bryan. "A Prospective Evaluation of Benzodiazepine Guidelines in the Management of Patients Hospitalized for Alcohol Withdrawal." Pharmacotherapy: The Journal of Human Pharmacology and Drug Therapy 14, no. 5 (1994): 579–85. http://dx.doi.org/10.1002/j.1875-9114.1994.tb02854.x.

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Our institution adopted guidelines for the selection of benzodiazepines to be administered to patients hospitalized for alcohol withdrawal. We assessed the guidelines' impact on prescribing habits, benzodiazepine dosage requirements and costs, and length of intensive care unit (ICU) stay. A 6‐month prospective, observational study was performed in 50 patients who exhibited signs of alcohol withdrawal and received benzodiazepine therapy. Appropriate therapy was defined as lorazepam for patients 60 years and older or those with hepatic dysfunction, and chlordiazepoxide for all other patients. Be
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7

Jawaro, Tara, Ayan Kumar, Oleksandr Pistun, and Deepali Dixit. "Stevens-Johnson Syndrome Associated With Chlordiazepoxide." Journal of Pharmacy Technology 34, no. 2 (2018): 82–85. http://dx.doi.org/10.1177/8755122517753595.

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Objective: To report a case of chlordiazepoxide-associated Stevens-Johnson syndrome (SJS). Case Summary: This case provides insight into a serious adverse drug reaction secondary to a drug not commonly associated with SJS. A 29-year-old female presented with a 4-day history of rash and pruritus. The rash started on her arms and spread all over her body. The patient was started on chlordiazepoxide 3½ weeks ago. On examination, there were multiple, raised, round erythematous lesions in various stages of healing. Skin erosions were noted on her lips and buccal mucosa. However, the rash did not in
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8

Nisbett, Khalin E., Leandro F. Vendruscolo, and George F. Koob. "Indulging Curiosity: Preliminary Evidence of an Anxiolytic-like Effect of Castor Oil and Ricinoleic Acid." Nutrients 16, no. 10 (2024): 1527. http://dx.doi.org/10.3390/nu16101527.

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In the process of validating the elevated zero maze, a common test of anxiety-like behavior, in our laboratory, we demonstrated an anxiolytic-like effect of castor oil and its primary component, ricinoleic acid. We tested the effects of vehicle and chlordiazepoxide in male mice in the elevated zero maze following a 30-min pretreatment time. Chlordiazepoxide is a United States Food and Drug Administration-approved drug that was previously shown to exert anxiolytic-like effects in both the elevated zero maze and elevated plus maze. Chlordiazepoxide was administered at doses of 5 or 10 mg/kg. We
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9

&NA;. "Chlordiazepoxide/clidinium bromide." Reactions Weekly &NA;, no. 868 (2001): 8. http://dx.doi.org/10.2165/00128415-200108680-00018.

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10

Fischer, Andreas. "Chlordiazepoxide dichloromethane monosolvate." Acta Crystallographica Section E Structure Reports Online 68, no. 4 (2012): o1011. http://dx.doi.org/10.1107/s1600536812009695.

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In the title compound (systematic name: 7-chloro-2-methylamino-5-phenyl-3H-1,4-benzodiazepine 4-oxide dichloromethane monosolvate), C16H14ClN3O·CH2Cl2, the seven-membered ring adopts a boat conformation with the CH2group as the prow and the two aromatic C atoms as the stern. The dihedral angle between the benzene rings is 75.25 (6)°. The crystal structure features centrosymmetric pairs of chlordiazepoxide molecules linked by pairs of N—H...O hydrogen bonds, which generateR22(12) loops.
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11

Salter, Mark. "Chlormethiazole or chlordiazepoxide?" Psychiatric Bulletin 21, no. 3 (1997): 186. http://dx.doi.org/10.1192/pb.21.3.186-a.

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12

Jagota, N. K., and J. T. Stewart. "Separation of Chlordiazepoxide and Selected Chlordiazepoxide Mixtures Using Capillary SFC." Journal of Liquid Chromatography 16, no. 2 (1993): 291–305. http://dx.doi.org/10.1080/10826079308020913.

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13

Singh, Ranapartap, Chawla Pooja, and Ravindra K. Rawal. "DEVELOPMENT AND VALIDATION OF ANALYTICAL METHOD FOR SIMULTANEOUS ESTIMATION OF CLIDINIUM BROMIDE, RABEPRAZOLE, CHLORDIAZEPOXIDE AND DICYCLOMINE HYDROCHLORIDE." INDIAN DRUGS 58, no. 07 (2021): 69–71. http://dx.doi.org/10.53879/id.58.07.12140.

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Clidinium bromide, rabeprazole sodium, chlordiazepoxide and dicyclomine hydrochloride(COLIWIN-R) drug combinations are used for the treatment of gastric acidity, anxiety, intestinal ulcers, abdominal cramps, irritable bowel syndrome and abdominal pain. A high performance liquid chromatographic method has been developed and validated for the simultaneous determination of clidinium bromide, rabeprazole sodium, chlordiazepoxide and dicyclomine hydrochloride in capsules dosage forms using WATERS C18 column (50 mm × 4.6 mm, 5 µm) with mobile phase consisting of methanol, acetonitrile and phosphate
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14

Khatereh, Mandanizadeh Mehrdad Modaresi *. Ilnaz Sajjadian. "COMPARING THE EFFECT OF HAWTHORN'S EXTRACT AND CHLORDIAZEPOXIDE ON REDUCING ANXIETY IN LABORATORY MICE." INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES 05, no. 05 (2018): 4435–40. https://doi.org/10.5281/zenodo.1255706.

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<em>Anxiety is a natural feeling which is experienced in threatening situations and can affect the physiology of the nervous system. The aim of this study was to compare the effect of hawthorn and chlordiazepoxide on reducing anxiety in mice. Sixty female mice in the weight range of 25 to 30g were divided into six groups of control, anxiety, chlordiazepoxide and 50, 100, and 200 mg/kg doses of hawthorn extract. After receiving the last dose, Anxiety was induced by the dark box and then was evaluated using plus evaluated maze. Animals were placed in a box with black walls for five minutes. Afte
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15

Chan, Arthur W. K., Donna L. Schanley, Michele C. Langan, Florence W. Leong, and Maria L. Penetrante. "Chronic treatment with ethanol or chlordiazepoxide alters the metabolism of chlordiazepoxide." Pharmacology Biochemistry and Behavior 35, no. 2 (1990): 363–66. http://dx.doi.org/10.1016/0091-3057(90)90170-m.

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16

Muchhala, Snehal, Seema Bhagat, Rahul Rathod, Amey Mane, and Bhavesh Kotak. "Safety and effectiveness of fixed dose combination of amitriptyline and chlordiazepoxide (Libotryp® and Libotryp-DS®) in the management of depression with co-morbid anxiety: protocol and design of a prospective, single arm, multi-centric, PMS study." International Journal of Clinical Trials 9, no. 3 (2022): 221. http://dx.doi.org/10.18203/2349-3259.ijct20221875.

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&lt;p&gt;&lt;strong&gt;Background:&lt;/strong&gt; Depression and anxiety are most disabling psychiatric conditions and add significantly to global health-related burden. Lifetime prevalence of major depression and anxiety disorders are very common and many times they can co-exist in the same time frame. The outcomes are poorer in such situations and compliance to medication is key to improve prognosis. A combination of tricyclic antidepressants and benzodiazepine is more practical in terms of compliance, and advantageous than that of a single class of drugs for the management of depression wit
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17

Parsa, Yekta, Zahra Nadia Sharifi, Fariborz Ghaffarpasand, et al. "Neurotoxicologically Outcomes of Perinatal Chlordiazepoxide Exposure on the Fetal Prefrontal Cortex Cells in Rat Pup." Galen Medical Journal 14 (July 2, 2025): e3649. https://doi.org/10.31661/gmj.v14i.3649.

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Background: Chlordiazepoxide is a benzodiazepine which is widely used as an anxiolytic, sedative and muscle-relaxant and its effects on neurodevelopment is yet to be identified. The aim of the current experimental study was to determine the effects of prenatal exposure to chlordiazepoxide on development of the prefrontal cortex (PFC). Materials and Methods: A total number of 9 pregnant Wister rats that were randomly assigned to three groups receiving standard rat food and drinking water ad libitum (n=3) or chlordiazepoxide (10 mg/kg) (n=3) and an equal volume of vehicle (0.9% NaCl) (n=3) intra
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18

Patel, Sejal K., and Natvarlal J. Patel. "Simultaneous Determination of Imipramine Hydrochloride and Chlordiazepoxide in Pharmaceutical Preparations by Spectrophotometric, RP-HPLC, and HPTLC Methods." Journal of AOAC INTERNATIONAL 93, no. 3 (2010): 904–10. http://dx.doi.org/10.1093/jaoac/93.3.904.

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Abstract A binary mixture of imipramine HCl and chlordiazepoxide was determined by three different methods. The first involved determination of imipramine HCl and chlordiazepoxide using the first derivative spectrophotometric technique at 219 and 231.5 nm over the concentration ranges of 120 and 224 g/mL with mean accuracies of 99.47 0.78 and 101.43 1.20, respectively. The second method utilized RP-HPLC with methanolacetonitrile0.065 M ammonium acetate buffer (45 + 25 + 30, v/v/v, pH adjusted to 5.6 0.02 with phosphoric acid) as the mobile phase pumped at a flow rate of 1.0 mL/min. Quantificat
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19

Dinarvand, Amin, Mehrdad Hashemi, Rasoul Dinarvand, Shabnam Movassaghi, and Mojtaba Jafarinia. "The Effect of Chlordiazepoxide Consumption on the Hippocampus of Neonatal Rats During Pregnancy." Galen Medical Journal 11 (December 13, 2022): e2283. http://dx.doi.org/10.31661/gmj.v11i.2283.

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Background: Chlordiazepoxide is an anti-anxiety drug commonly used by young people and pregnant women to reduce anxiety. The adverse effects of this drug on cholinergic nervous system function have been demonstrated. Therefore, in this study, the effect of chlordiazepoxide consumption during pregnancy was evaluated on the rats infant hippocampus. Materials and Methods: Nine pregnant Wistar rats were randomly divided (n=3 per group) into control, experimental (daily intraperitoneal injection of chlordiazepoxide at a dose of 10 mg/kg for 21 days), and vehicle (same amount of normal saline) group
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20

Young, Simon, and Bryan G. Walpole. "Tranylcypromine and chlordiazepoxide intoxication." Medical Journal of Australia 144, no. 3 (1986): 166–67. http://dx.doi.org/10.5694/j.1326-5377.1986.tb112261.x.

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21

&NA;. "Chlordiazepoxide/clidinium bromide overdose." Reactions Weekly &NA;, no. 1262 (2009): 10. http://dx.doi.org/10.2165/00128415-200912620-00029.

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22

&NA;. "Chlordiazepoxide/fenproporex/fluoxetine abuse." Reactions Weekly &NA;, no. 1306 (2010): 15. http://dx.doi.org/10.2165/00128415-201013060-00051.

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23

Entwistle, N., P. Owen, D. A. Patterson, L. V. Jones, and J. A. Smith. "The Occurrence of Chlordiazepoxide Degradation Products in Sudden Deaths Associated with Chlordiazepoxide Overdosage." Journal of the Forensic Science Society 26, no. 1 (1986): 45–54. http://dx.doi.org/10.1016/s0015-7368(86)72445-6.

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24

Hoey, Lori L., Avi Nahum, and Kyle Vance‐Bryan. "A Retrospective Review and Assessment of Benzodiazepines in the Treatment of Alcohol Withdrawal in Hospitalized Patients." Pharmacotherapy: The Journal of Human Pharmacology and Drug Therapy 14, no. 5 (1994): 572–78. http://dx.doi.org/10.1002/j.1875-9114.1994.tb02853.x.

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Little information has been published concerning differences among the benzodiazepines in treating hospitalized patients with severe symptoms of alcohol withdrawal. We attempted to determine the length and type of hospital stay, and the pattern and appropriateness of administration, dosage requirements, and costs associated with benzodiazepines in patients undergoing alcohol withdrawal. A 1‐year retrospective analysis was performed for 57 hospitalized patients. Appropriate therapy was defined as lorazepam for patients 60 years and older or those with hepatic dysfunction, and chlordiazepoxide o
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25

Day, Ed, Jaimin Patel, and George Georgiou. "Evaluation of a symptom-triggered front-loading detoxification technique for alcohol dependence: A pilot study." Psychiatric Bulletin 28, no. 11 (2004): 407–10. http://dx.doi.org/10.1192/pb.28.11.407.

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Aims and MethodsA pilot study was set up to compare a symptom-triggered ‘front-loading’ detoxification technique with the usual fixed dosage method. A group of 23 in-patients with alcohol dependence were randomised to receive either the intervention technique using diazepam or the standard chlordiazepoxide taper over 10 days.ResultsThe intervention group received a mean dosage of 74 mg diazepam (equivalent to 222 mg chlordiazepoxide) compared with 700 mg chlordiazepoxide in those receiving usual treatment. There was no statistical difference in the severity of alcohol withdrawal symptoms in th
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26

Khodadoust, Saeid, Tahereh Nasiriani, and Fatemeh Zeraatpisheh. "Preparation of a magnetic molecularly imprinted polymer for the selective adsorption of chlordiazepoxide and its determination by central composite design optimized HPLC." New Journal of Chemistry 42, no. 17 (2018): 14444–52. http://dx.doi.org/10.1039/c8nj02643b.

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27

Wallace, IR, EC Campbell, and Micheal Trimble. "Use of a flumazenil infusion to treat chlordiazepoxide toxicity." Acute Medicine Journal 16, no. 1 (2017): 30–34. http://dx.doi.org/10.52964/amja.0649.

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“Alcohol detox” is a common presentation to acute medical services and is usually managed via standardised guidelines and protocols. We present a case of chlordiazepoxide toxicity, requiring repeated bolus doses and subsequently 24 hours of an intravenous infusion of flumazenil in response to guideline directed management of an alcohol withdrawal state. The use of prolonged flumazenil infusions to treat benzodiazepine toxicity is infrequently described. Chlordiazepoxide is metabolised in the hepatic microsomal pathway and hepatic impairment can lead to accumulation of toxic metabolites, which
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28

Curzon, G., G. A. Kennett, G. S. Sarna, and P. S. Whitton. "The Effects of Tianeptine and other Antidepressants on a Rat Model of Depression." British Journal of Psychiatry 160, S15 (1992): 51–55. http://dx.doi.org/10.1192/s0007125000296682.

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A model of depression based on measurements made after restraining rats for two hours has been developed. The model is associated with elevation in corticosterone, reflects the higher incidence of depression in women, and shows increased post-synaptic 5-HT function with adaptation. The effects of tianeptine and other antidepressants on the model were studied. Chronic pre-treatment with desipramine, sertraline (amine uptake inhibitors), and chlordiazepoxide normalised open field activity after restraint. Single high doses, post-restraint, of 8-OH-DPAT, gepirone (5-HT agonists), and tianeptine n
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29

Heuschele, Walter P. "CHLORDIAZEPOXIDE FOR CALMING ZOO ANIMALS." International Zoo Yearbook 3, no. 1 (2008): 116–19. http://dx.doi.org/10.1111/j.1748-1090.1962.tb03429.x.

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30

Huang, Po-Hsun, and Wei-Jen Tsai. "Chlordiazepoxide-induced Stevens-Johnson Syndrome." Journal of the Chinese Medical Association 68, no. 6 (2005): 276–78. http://dx.doi.org/10.1016/s1726-4901(09)70150-9.

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31

Tonkiss, John, Penny L. Shultz, Jed S. Shumsky, et al. "Chlordiazepoxide-Induced Spatial Learning Deficits." Pharmacology Biochemistry and Behavior 65, no. 1 (2000): 105–16. http://dx.doi.org/10.1016/s0091-3057(99)00182-3.

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32

Howells, Roger. "Chlordiazepoxide dosage for alcohol withdrawal." Psychiatric Bulletin 24, no. 9 (2000): 354. http://dx.doi.org/10.1192/pb.24.9.354-a.

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33

Garbutt, James C., Gregory M. Gillette, and Robert E. Hicks. "TRH effect on chlordiazepoxide sedation." Biological Psychiatry 25, no. 7 (1989): 983–85. http://dx.doi.org/10.1016/0006-3223(89)90285-0.

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34

Woudenberg, Fred, and Theo H. Hijzen. "Discriminated taste aversion with chlordiazepoxide." Pharmacology Biochemistry and Behavior 39, no. 4 (1991): 859–63. http://dx.doi.org/10.1016/0091-3057(91)90044-3.

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35

Sefid-Sefidehkhan, Yasaman, Zahra Karimzadeh, Abolghasem Jouyban, Maryam Khoubnasabjafari, Vahid Jouyban-Gharamaleki, and Elaheh Rahimpour. "Development of a nanocomposite hydrogel catalyzed H2O2/TMB system for determination of chlordiazepoxide in exhaled breath condensate." RSC Advances 14, no. 40 (2024): 29143–50. http://dx.doi.org/10.1039/d4ra03751k.

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36

S., K. TIWAR, and M. SHARMA L. "Effect of Coordination on the Psychopharmacological Activity of Chlordiazepoxide. Part-I. Copper(II) and Zinc(II) Complexes." Journal of Indian Chemical Society Vol. 73, Nov 1996 (1996): 600–601. https://doi.org/10.5281/zenodo.5917968.

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Department of Chemistry, N A S College, Meerut-250 001 <em>Manuscript received 17 March 1994, accepted 22 March 1995</em> Effect of Coordination on the Psychopharmacological Activity of Chlordiazepoxide. Part-I. Copper(II) and Zinc(II) Complexes.
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Sharma, Rajesh, Mukesh C. Sharma, and Gaurav Vijaywargiya. "DEVELOPMENT AND VALIDATION OF RP-HPLC METHOD FOR SIMULTANEOUS ESTIMATION OF CLIDINIUM BROMIDE, CHLORDIAZEPOXIDE AND DICYCLOMINE HYDROCHLORIDE IN TABLET DOSAGE FORM." INDIAN DRUGS 58, no. 4 (2021): 78–81. http://dx.doi.org/10.53879/id.58.04.11255.

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A simple, specific, accurate reversed phase high performance liquid chromatographic method was developed for the simultaneous estimation of clidinium bromide, chlordiazepoxide and dicyclomine hydrochloride. Chromatographic separation of the three drugs was performed on a Chromatopak C-18 column (25 cm x 4.6 i.d. x 5µm) as the stationary phase with a mobile phase composed of 0.1 % triethylamine in water pH adjusted by 5 % o-phosphoric acid and acetonitrile in the ratio 30:70 at a flow rate of 0.8mL/min, Detection was carried out at 210 nm. The retention times of clidinium bromide, chlordiazepox
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38

Motaharian, Ali, and Mohammad Reza Milani Hosseini. "Electrochemical sensor based on a carbon paste electrode modified by graphene nanosheets and molecularly imprinted polymer nanoparticles for determination of a chlordiazepoxide drug." Analytical Methods 8, no. 33 (2016): 6305–12. http://dx.doi.org/10.1039/c6ay01594h.

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Procedure for fabrication of electrochemical sensor based on carbon paste electrode modified with molecularly imprinted polymer nanoparticles and graphene nanosheets for selective and sensitive determination of chlordiazepoxide (CDP) drug.
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39

Ahmed, Nief Rahman. "High Performance Liquid Chromatographic Method for the Determination of Chlordiazepoxide in Pharmaceutical Preparations Application to content uniformity testing." Al Mustansiriyah Journal of Pharmaceutical Sciences 17, no. 2 (2018): 7. http://dx.doi.org/10.32947/ajps.v17i2.44.

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A reverse phase high performance liquid chromatographic method (HPLC) has been developed for the determination of chlordiazepoxide in the pharmaceutical formulations . Separation was achieved using supelco C18 column(25cm x 4.6 mm. 5 µm). The mobile phase (ethanol), adjusted pH to 1.0 with 1N sulfuric acid and pumped at a flow rate of 1.0 ml/min . The peaks were detected at 310 nm. Linearity was obtained in the concentration range of 0.01- 0.20 mg/ml .The method was statistically validated and RSD was found to be less than 1.5 % indicating high degree of accuracy and precision of the proposed
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40

Pratap, Dr Nitesh. "Efficacy of Clidinium and Chlordiadepoxide as Add-On Therapy in Gastric Disorders." International Journal for Research in Applied Science and Engineering Technology 13, no. 5 (2025): 722–24. https://doi.org/10.22214/ijraset.2025.68930.

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Background and Aim: The treatment of Gastric disorders is a challenge. Clidinium/chlordiazepoxide is a combination of antispasmodic and anxiolytic drugs that has been used as an adjunct treatment for GERD, Functional Dyspepsia, and Organic dyspepsia in clinical practice with limited supporting evidence of efficacy. The study aims to assess the efficacy and safety of clidinium/chlordiazepoxide as an adjunct treatment to a proton pump inhibitor (PPI) in refractory dyspepsia. Materials and Methods: This prospective, observational, and comparative study was conducted in outpatient and inpatient un
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41

Alkhuzaim, OsamahM. "Lichenoid drug eruption induced by chlordiazepoxide." Journal of Dermatology and Dermatologic Surgery 26, no. 3 (2022): 29. http://dx.doi.org/10.4103/jdds.jdds_35_20.

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42

Thorn, Ingrid. "Primidone and Chlordiazepoxide in Cerebral Palsy." Developmental Medicine & Child Neurology 4, no. 3 (2008): 325–27. http://dx.doi.org/10.1111/j.1469-8749.1962.tb03175.x.

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43

Singh, Dilraj, Peter V. Marshall, Len Shields, and Peter York. "Solid-State Characterization of Chlordiazepoxide Polymorphs." Journal of Pharmaceutical Sciences 87, no. 5 (1998): 655–62. http://dx.doi.org/10.1021/js960385c.

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44

Medeiros, Bruno C., and Jeffrey H. Lipton. "Chlordiazepoxide for imatinib-induced muscular cramps." European Journal of Haematology 77, no. 6 (2006): 538. http://dx.doi.org/10.1111/j.1600-0609.2006.00742.x.

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45

Diesen, Veronica, Cláudio Lousada, and Andreas Fischer. "A hydrogen sulfate salt of chlordiazepoxide." Acta Crystallographica Section E Structure Reports Online 68, no. 7 (2012): o2091—o2092. http://dx.doi.org/10.1107/s1600536812024920.

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46

Barton, K., P. W. Auld, M. G. Scott, and D. P. Nicholls. "Chlordiazepoxide Metabolite Accumulation in Liver Disease." Medical Toxicology 4, no. 1 (1989): 73–76. http://dx.doi.org/10.1007/bf03259904.

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47

Chan, Arthur W. K., Donna L. Schanley, Michael D. Aleo, and Florence W. Leong. "Cross-tolerance between ethanol and chlordiazepoxide." Alcohol 2, no. 2 (1985): 209–13. http://dx.doi.org/10.1016/0741-8329(85)90047-3.

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48

Flaherty, Charles F., Grace A. Rowan, and Larissa A. Pohorecky. "Corticosterone, novelty-induced hyperglycemia, and chlordiazepoxide." Physiology & Behavior 37, no. 3 (1986): 393–96. http://dx.doi.org/10.1016/0031-9384(86)90196-4.

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49

Mittal, S. R., and A. K. Mathur. "Drug interaction between metoprolol and chlordiazepoxide." International Journal of Cardiology 13, no. 3 (1986): 372–74. http://dx.doi.org/10.1016/0167-5273(86)90123-3.

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50

Colpaert, F. C., and W. Koek. "Behavioural specificity of chlordiazepoxide-produced StD." Behavioural Pharmacology 7, no. 1 (1996): 49???55. http://dx.doi.org/10.1097/00008877-199601000-00004.

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