Tahir Jamshaid, S. S. Hassan, Hammad Ahmed, M. A. U. Rehman
The purpose of the study is to develop and validate method for assay of Aceclofenac in tablet dosage forms using ultra violet spectrophotometry (UV) and high performance liquid chromatography (HPLC) techniques. A method was developed and validated for analysis of Aceclofenac using UV technique with methanol and phosphate buffer 7.4 as solvent. The HPLC analysis was conducted using two mobile phases, that is, “A” as Acetonitrile: Methanol (80:20 v/v) and “B” as Acetonitrile: methanol: NH3 solution (225:50:1 v/v/v). The method was used for assay determination for tablets dosage forms and results were found to be in compliance with official standards. Validation studies were also carried out for both methods. Linearity, LOD, single point calibration, precision and accuracy and % RSD were calculated. Aceclofenac standard was analysed with UV Spectrophotometer in the concentration ranges of 0.5-50 and 0.4-50 mg/L for each solvent and results showed good linearity with R2 = 0.9998 and 0.9999. The method was also specific that verifies the absence of interference at the max of Aceclofenac. UV analysis was precise with % RSD falling within 2% and LOD as 0.5 and 0.4 mg/L for methanol and PBS 7.4, respectively. The tablets of three brands showed assay percentages within specified limits in methanol (109.33, 103.90 and 105.61%) and PBS 7.4 (108.70, 100.69 and 106.60%). In HPLC analysis, mobile phase ‘B’ showed more sharp peaks with lesser HETP and Tf compared to mobile phase ‘A’. The method was checked for reliability and efficiency for assay and some of the parameters like height efficiency to theoretical plates (HETP), tailing factor, peak heights, peak widths along with validation studies (Linearity range 0.1-50 mg/L, specificity, precision, and limit of detection and single point calibration). The more basic mobile phase B using NH3 solution produced more sharp peaks as compared to less basic mobile phase A. Key words: Aceclofenac, UV-Visible spectrophotometry, high performance liquid chromatography (HPLC), validation.
{"title":"Development and validation of UV- Spectrophotometric and RP-HPLC method for the analysis of raw material and formulations of Aceclofenac","authors":"Tahir Jamshaid, S. S. Hassan, Hammad Ahmed, M. A. U. Rehman","doi":"10.5897/ajpp2020.5163","DOIUrl":"https://doi.org/10.5897/ajpp2020.5163","url":null,"abstract":"The purpose of the study is to develop and validate method for assay of Aceclofenac in tablet dosage forms using ultra violet spectrophotometry (UV) and high performance liquid chromatography (HPLC) techniques. A method was developed and validated for analysis of Aceclofenac using UV technique with methanol and phosphate buffer 7.4 as solvent. The HPLC analysis was conducted using two mobile phases, that is, “A” as Acetonitrile: Methanol (80:20 v/v) and “B” as Acetonitrile: methanol: NH3 solution (225:50:1 v/v/v). The method was used for assay determination for tablets dosage forms and results were found to be in compliance with official standards. Validation studies were also carried out for both methods. Linearity, LOD, single point calibration, precision and accuracy and % RSD were calculated. Aceclofenac standard was analysed with UV Spectrophotometer in the concentration ranges of 0.5-50 and 0.4-50 mg/L for each solvent and results showed good linearity with R2 = 0.9998 and 0.9999. The method was also specific that verifies the absence of interference at the max of Aceclofenac. UV analysis was precise with % RSD falling within 2% and LOD as 0.5 and 0.4 mg/L for methanol and PBS 7.4, respectively. The tablets of three brands showed assay percentages within specified limits in methanol (109.33, 103.90 and 105.61%) and PBS 7.4 (108.70, 100.69 and 106.60%). In HPLC analysis, mobile phase ‘B’ showed more sharp peaks with lesser HETP and Tf compared to mobile phase ‘A’. The method was checked for reliability and efficiency for assay and some of the parameters like height efficiency to theoretical plates (HETP), tailing factor, peak heights, peak widths along with validation studies (Linearity range 0.1-50 mg/L, specificity, precision, and limit of detection and single point calibration). The more basic mobile phase B using NH3 solution produced more sharp peaks as compared to less basic mobile phase A. \u0000 \u0000 Key words: Aceclofenac, UV-Visible spectrophotometry, high performance liquid chromatography (HPLC), validation.","PeriodicalId":7531,"journal":{"name":"African Journal of Pharmacy and Pharmacology","volume":"14 1","pages":"259-277"},"PeriodicalIF":0.0,"publicationDate":"2020-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.5897/ajpp2020.5163","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45816169","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Tohidul Amin Mohammad, Fatema Kaniz, Karmakar Palash, A. Md., Haque Tazmel, Shahabuddin Kabir Choudhuri M.
The ayurvedic medicinal system is the world’s most primitive medical systems which were originated in India. For the treatment of Sprue syndrome, a very well-known ayurvedic preparation named Kutajarista (KTJ) is used in the south Asian region. This study aimed to detect the impact of chronic administration of KTJ on hematological parameters. The experimental animals were subdivided into two groups. A high dose (50 mL/kg) of body weight was given to the first group for 42 days and the second group which was considered as the control group was treated with normal water for the same period. There was a remarkable reduction [10.37%, p=0.092] in the total numbers of red blood cells (RBC). A prominent decrease [10.75%. p=0.097] is also observed in the hemoglobin content of the blood. There was a noticeable [11.05%, p=0.077] decrease in the hematocrit level of the blood and a very high [64.35%, p=0.19] increase in the number of white blood cell (WBC) count of the male Sprague-Dawley rat. A remarkably high increase was observed in the absolute count of Neutrophils (220.161%, p=0.12), Eosinophils (368.75%, p=0.11), Lymphocytes [11.29%, p=0.06], and Monocyte [142.781%, p=0.13] count. Also a prominent [↑ 14.15%, p=0.42] increase in the number of platelet counts was observed. Rat cutaneous tail bleeding time and whole blood clotting time shortening were also observed and the result is statistically prominent. As the result shows a significant change in different hematological parameter it can be summarized that KTJ have potential hemotoxicity at a higher dose. Further study is required at a lower dose. Key words: Ayurvedic, Kutajarista, hemotoxicity, red blood cells (RBC), white blood cells (WBC).
{"title":"Investigation of hemotoxicologic potential of an ayurvedic preparation Kutajarista used in Sprue syndrome after chronic administration to male Sprague-Dawley rats","authors":"Tohidul Amin Mohammad, Fatema Kaniz, Karmakar Palash, A. Md., Haque Tazmel, Shahabuddin Kabir Choudhuri M.","doi":"10.5897/ajpp2020.5174","DOIUrl":"https://doi.org/10.5897/ajpp2020.5174","url":null,"abstract":"The ayurvedic medicinal system is the world’s most primitive medical systems which were originated in India. For the treatment of Sprue syndrome, a very well-known ayurvedic preparation named Kutajarista (KTJ) is used in the south Asian region. This study aimed to detect the impact of chronic administration of KTJ on hematological parameters. The experimental animals were subdivided into two groups. A high dose (50 mL/kg) of body weight was given to the first group for 42 days and the second group which was considered as the control group was treated with normal water for the same period. There was a remarkable reduction [10.37%, p=0.092] in the total numbers of red blood cells (RBC). A prominent decrease [10.75%. p=0.097] is also observed in the hemoglobin content of the blood. There was a noticeable [11.05%, p=0.077] decrease in the hematocrit level of the blood and a very high [64.35%, p=0.19] increase in the number of white blood cell (WBC) count of the male Sprague-Dawley rat. A remarkably high increase was observed in the absolute count of Neutrophils (220.161%, p=0.12), Eosinophils (368.75%, p=0.11), Lymphocytes [11.29%, p=0.06], and Monocyte [142.781%, p=0.13] count. Also a prominent [↑ 14.15%, p=0.42] increase in the number of platelet counts was observed. Rat cutaneous tail bleeding time and whole blood clotting time shortening were also observed and the result is statistically prominent. As the result shows a significant change in different hematological parameter it can be summarized that KTJ have potential hemotoxicity at a higher dose. Further study is required at a lower dose. \u0000 \u0000 Key words: Ayurvedic, Kutajarista, hemotoxicity, red blood cells (RBC), white blood cells (WBC).","PeriodicalId":7531,"journal":{"name":"African Journal of Pharmacy and Pharmacology","volume":"14 1","pages":"308-315"},"PeriodicalIF":0.0,"publicationDate":"2020-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.5897/ajpp2020.5174","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44184388","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
S. Ghasi, I. Umana, A. Ogbonna, M. Nwokike, Sa Ufelle
The present study was designed to investigate the cardioprotective effect of animal grade piperazine citrate on isoproterenol-induced myocardial infarction in rats by studying cardiac marker enzymes and histopathological changes of the cardiac muscle. Isoproterenol administration showed significant (P<0.001) increase in the serum levels of cardiac injury markers (creatine kinase-MB and troponin-I), 358.98 ± 7.68 iu/l and 13.16 ± 0.35 ng/ml compared to the normal control group of 291.58 ± 3.56 iu/l and 9.66 ± 0.20 ng/ml respectively. Pretreatment with 15 and 30 mg/kg body weight of piperazine citrate showed a decrease in the troponin-I levels when compared with the isoproterenol group; 13.16 ± 0.35 to 12.39 ± 0.22 ng/ml in the group that received 15 mg/kg piperazine citrate (p = 0.0881) and 13.16 ± 0.35 to 11.79 ± 0.30 ng/ml (p = 0.0132) in case of the group pretreated with 30 mg/kg piperazine citrate. With regards to CK-MB, the treated groups with piperazine citrate 15 and 30 mg/kg body weight showed a reduction in the values, 340.76 ± 5.10 (p = 0.0763) and 344.17 ± 8.24 iu/l (p = 0.2178) respectively, compared to the isoproterenol group value of 358.98 ± 7.68 iu/l. Histopathological investigation showed that there was no significant architectural changes in the normal control group that received only normal saline. Structural aberrations caused by isoproterenol were also significantly reduced in the piperazine citrate treated groups. Therefore, the results of the present study suggest that low dose piperazine citrate has a significant effect on the protection of the heart. Key words: Piperazine citrate, myocardial infarction, histopathology, Wistar rat.
{"title":"Cardioprotective effects of animal grade piperazine citrate on isoproterenol induced myocardial infarction in wistar rats: Biochemical and histopathological evaluation","authors":"S. Ghasi, I. Umana, A. Ogbonna, M. Nwokike, Sa Ufelle","doi":"10.5897/ajpp2020.5164","DOIUrl":"https://doi.org/10.5897/ajpp2020.5164","url":null,"abstract":"The present study was designed to investigate the cardioprotective effect of animal grade piperazine citrate on isoproterenol-induced myocardial infarction in rats by studying cardiac marker enzymes and histopathological changes of the cardiac muscle. Isoproterenol administration showed significant (P<0.001) increase in the serum levels of cardiac injury markers (creatine kinase-MB and troponin-I), 358.98 ± 7.68 iu/l and 13.16 ± 0.35 ng/ml compared to the normal control group of 291.58 ± 3.56 iu/l and 9.66 ± 0.20 ng/ml respectively. Pretreatment with 15 and 30 mg/kg body weight of piperazine citrate showed a decrease in the troponin-I levels when compared with the isoproterenol group; 13.16 ± 0.35 to 12.39 ± 0.22 ng/ml in the group that received 15 mg/kg piperazine citrate (p = 0.0881) and 13.16 ± 0.35 to 11.79 ± 0.30 ng/ml (p = 0.0132) in case of the group pretreated with 30 mg/kg piperazine citrate. With regards to CK-MB, the treated groups with piperazine citrate 15 and 30 mg/kg body weight showed a reduction in the values, 340.76 ± 5.10 (p = 0.0763) and 344.17 ± 8.24 iu/l (p = 0.2178) respectively, compared to the isoproterenol group value of 358.98 ± 7.68 iu/l. Histopathological investigation showed that there was no significant architectural changes in the normal control group that received only normal saline. Structural aberrations caused by isoproterenol were also significantly reduced in the piperazine citrate treated groups. Therefore, the results of the present study suggest that low dose piperazine citrate has a significant effect on the protection of the heart. \u0000 \u0000 Key words: Piperazine citrate, myocardial infarction, histopathology, Wistar rat.","PeriodicalId":7531,"journal":{"name":"African Journal of Pharmacy and Pharmacology","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2020-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.5897/ajpp2020.5164","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42135466","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A. Fahd, M. Omar, A. Ramzi, Suwayda Ali, A. Abdullah
Cancer and microbial infectious diseases are considered a global threat. Plants have been investigated across the world to exploit their potential anticancer and antimicrobial effective agents. In this study, two medicinal plant species native to Saudi Arabia, namely; Artemisia judaica and Artemisia sieberi were screened to assess their antioxidant, anticancer and antimicrobial potential activities as well as phytochemical compositions. The collected aerial parts were extracted by maceration with methanol. Cytotoxic and antimicrobial activities were investigated using the MTT and MIC assays, respectively. Free radical scavenging and antioxidant potential were assessed respectively by 2, 2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid (ABTS) methods. The total flavonoid and phenolic contents of the crude methanolic extract were quantified using standard methods. Artemisia judaica displayed a strong cytotoxicity compared to A. sieberi while both species showed approximately similar bacterial and fungal growth inhibition. In contrast, A. sieberi displayed the highest phenol and flavonoid contents between the two species which was consistent with the higher antioxidant activity found in A. sieberi. It is concluded that both Artemisia species could be a promising source of antioxidant, anticancer and antimicrobial agents. Key words: Artemisia judaica, Artemisia sieberi, anticancer, antimicrobial.
{"title":"Cytotoxic, antimicrobial and antioxidant activities and phytochemical analysis of Artemisia judaica and \u0000A. sieberi in Saudi Arabia","authors":"A. Fahd, M. Omar, A. Ramzi, Suwayda Ali, A. Abdullah","doi":"10.5897/ajpp2020.5175","DOIUrl":"https://doi.org/10.5897/ajpp2020.5175","url":null,"abstract":"Cancer and microbial infectious diseases are considered a global threat. Plants have been investigated across the world to exploit their potential anticancer and antimicrobial effective agents. In this study, two medicinal plant species native to Saudi Arabia, namely; Artemisia judaica and Artemisia sieberi were screened to assess their antioxidant, anticancer and antimicrobial potential activities as well as phytochemical compositions. The collected aerial parts were extracted by maceration with methanol. Cytotoxic and antimicrobial activities were investigated using the MTT and MIC assays, respectively. Free radical scavenging and antioxidant potential were assessed respectively by 2, 2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid (ABTS) methods. The total flavonoid and phenolic contents of the crude methanolic extract were quantified using standard methods. Artemisia judaica displayed a strong cytotoxicity compared to A. sieberi while both species showed approximately similar bacterial and fungal growth inhibition. In contrast, A. sieberi displayed the highest phenol and flavonoid contents between the two species which was consistent with the higher antioxidant activity found in A. sieberi. It is concluded that both Artemisia species could be a promising source of antioxidant, anticancer and antimicrobial agents. \u0000 \u0000 Key words: Artemisia judaica, Artemisia sieberi, anticancer, antimicrobial.","PeriodicalId":7531,"journal":{"name":"African Journal of Pharmacy and Pharmacology","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2020-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.5897/ajpp2020.5175","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43075029","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}