1.Study on technical preparation of dexchlorpheniramine film coated tablets 6mg with sustained release
Pharmaceutical Journal 2000;291(7):15-18
Sustained release film coated tablets containing dexchlorpheniramine maleate were prepared in such a structure as two-third of drug were dispersed in Eudragit RS 100 to form insoluble matrix that gradually releases drug by diffusional mechanism, the rest was dispersed in the immediate release part. The core tablets were compressed by a wet granulation process and the film coated tablets by a routine film coating process with Eudragit E suspension. The formed coated tablets have suitable technical characteristics. The third formulation with Eudragit RS- drug ratio 2:1 has got the dissolution extent and the release rate in vitro similar to those of Polaramine 6mg repetabs. They also meet the requirements invitro release rate versus time for sustained release capsules containing Chlorpheniramine maleate by USP XXIII. Therefore, these film coated tablets with dexchlorpheniramine maleate may be candidates for a sustained release dosage form
dexchlorpheniramine
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Tablets
2.Dosage of metronidazole in tablets by HPLC in reverted phase:
Pharmaceutical Journal 1999;282(10):22-24
Quantitation of Metronidazole by reversed phase liquid chromatography using Supelco LC-ABZ column and a mobile phase containing an acid aqueous phase (pH
3.Preliminary study on application of some dosage methods of berberine chloride in raw material and berberin tablets
Pharmaceutical Journal 2005;0(1):22-24
Study on some methods used to quantify berberine chloride showed that the UV measuring and volumetric titration methods did not express only amount of berberine chloride itself. It is necessary to apply high- performance liquid chromatography (HPLC) to achieve the optimal conditions for better splitting, higher accuracy…in order to apply more widely in testing products commonly in market with many components combined to berberine chloride. To find out optimal methods, which are suitable with condition of present some pharmaceutical units, it is necessary to experiment continuously methods such as UV measuring and volumetric titration,… using HPLC method to compare.
Berberine
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Tablets
4.An Evaluation of Short-term Isoprodian Treatment in Leprosy.
Korean Journal of Dermatology 1977;15(3):267-277
Twenty-three bacteriologically positive leprosy patients were randomly selected from a leprosarium, randomly divided into four treatment groups, and given vaying dosages of Isoprodian, the tablet contained INAH 175mg, Prothionamide 175mg and DDS 50 mg, for five months. Group I: Initial 1/2 tablet dose per week with 1/2 tablet increment every weeks until 12 tablets were being consumed w.
Humans
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Leprosy*
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Prothionamide
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Tablets
5.Clinical Effects of Serenoa Repens(Permixon) on Chronic Prostatitis.
Jung Chul YUN ; Sang Kyu CHUNG
Korean Journal of Urology 1990;31(6):869-873
Chronic prostatitis has various symptoms and many problems in management. Recently a lipidosterolic extract of Serenoa Repens, Permixon has been reported to reveal potential antiandrogenic and anti inflammatory activities on prostate. Then we used Permixon on chronic prostatitis and following results were obtained. Permixon is administered orally in dose of 160mg., b.i.d. for 60 days in 31 cases of chronic prostatitis in 1st group, Permixon 160mg, with Cipro-floxacin 500mg, b.i.d. in 35 cases in 2nd group and Placebo 2 tablets, b.i.d. in 30 cases in 3rd group. In 1st group 36 cases(77.4%) were improved, 29 cases(82.8%) in 2nd group and 7 cases (23.3 %) of 3rd group were improved. Permixon is an effective drug in chronic prostatitis and there was no changes in laboratory findings and negligible side effects were noticed
Prostate
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Prostatitis*
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Serenoa*
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Tablets
6.A preparation of captopril sustained release tablet
Journal of Medical and Pharmaceutical Information 2004;0(8):28-31
to build formula of captopril sustained release matrix tablets with EC and HPMC, survey the affects of formulation components and optimization of formula by using D- Optimal. Subject: captopril, EC, HPMC, lactose, and starch. Method: prepare tablet, assess the quality of captopril sustained release matrix tablets. Conclusions: From the experiment design, captopril sustained release oral tablets with half life of 12h can be prepared, and by optimized method, the proper formula was found. To produce captopril tablets, it's necessary to further study in large scale, to perform test of bio-equivalence and stability of tablet
Captopril
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Tablets
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Pharmaceutical Preparations
7.Retrospective evaluation of the manufacture process of Oroken 200mg tablets
Pharmaceutical Journal 1999;370(8):16-18
GMP requires that all procedures should be properly validated...To ensure that processes and procedures remain capable of achieving the intended results, they should routinely undergo critical approvals. To obtain this purpose, the retrospective validation is proceeded with data provided from at least 10 batches. According to a C. Estampe study, we carried out a retrospective validation with Oroken 200mg tablets produced at the Saint Genis-Laval factory of Rh«ne-Poulenc Rorer (French).
Manufactured Materials
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Tablets
8.Clinical Evaluation of Cernilton in Chronic Prostatitis.
Korean Journal of Urology 1974;15(3):191-194
A microbiological extract of pollen, Cernilton was administered orally in dose of four tablets daily for 14 to 36 days in 25 cases of chronic prostatitis and following results were obtained. 1) Of the cases, 13 cases' (72%) Were improved and 7 cases(28%) were. not improved.. 2) No deleterious side effect were observed.
Pollen
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Prostatitis*
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Tablets
9.Clinical Evaluation of Cernilton in Chronic Prostatitis.
Korean Journal of Urology 1974;15(3):191-194
A microbiological extract of pollen, Cernilton was administered orally in dose of four tablets daily for 14 to 36 days in 25 cases of chronic prostatitis and following results were obtained. 1) Of the cases, 13 cases' (72%) Were improved and 7 cases(28%) were. not improved.. 2) No deleterious side effect were observed.
Pollen
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Prostatitis*
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Tablets
10.Preliminary assessment of the effect of CTK tablet on baterial utero-vaginitis
Journal of Practical Medicine 2003;442(2):53-55
The effect of Ha Noi College of Pharmacy producted CTK tablet containing 0.5g CTK mixed powder on bacterial utero-vaginitis was studied on 31 female married subjects aged 18-44. Chloramphenicol 0.25g tablet producted by Central pharmaceutical Factory N2 was used control. Results showed that CTK tablet manifests antibacterial effect compared with chloramphenicol in utero-vaginitis. Antibacterial effect is 65.4% by a dose of treatment (20 times of application of tablet). The effect of healing the lesion was manifested earlier than that of chateravaginitisull
Tablets
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Vaginitis
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Bacterial Infections