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Swathi, P.
- Combining Ability Studies for Fibre Quality Traits in Upland Cotton (Gossypium hirsutum L.)
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Authors
Affiliations
1 Department of Genetics and Plant Breeding, College of Agriculture, University of Agricultural Sciences, Dharwad, Karnataka, IN
2 Agricultural Research Station, (U.A.S.) Hebballi Farm, Dharwad, Karnataka, IN
3 Department of Agronomy, College of Agriculture, University of Agricultural Sciences, Dharwad, Karnataka, IN
1 Department of Genetics and Plant Breeding, College of Agriculture, University of Agricultural Sciences, Dharwad, Karnataka, IN
2 Agricultural Research Station, (U.A.S.) Hebballi Farm, Dharwad, Karnataka, IN
3 Department of Agronomy, College of Agriculture, University of Agricultural Sciences, Dharwad, Karnataka, IN
Source
International Journal of Plant Sciences, Vol 8, No 2 (2013), Pagination: 312-315Abstract
An investigation was carried out to assess the combining ability and nature of gene action in respect of seed cotton yield and its component traits in 54 new hybrids developed by crossing 9 lines with 6 testers of upland cotton in line × tester mating design in Randomized Block Design with two replications during Kharif 2010 at Main Agricultural Research Station, University of Agricultural Sciences, Dharwad. The variance among the lines (2.5 % span length and micronaire), testers and line × tester interaction (2.5 % span length, fibre strength and micronaire) were highly significant for the characters indicating predominance of non-additive gene action in genetic control of these traits. Magnitude of sca variance was higher than the gca variance for majority of the traits. The ratio of gca/ sca variance indicated preponderance of non-additive type of gene action, which is an integral component of the genetic architecture of different characters in the material used in cotton. L1 and L9 among the lines and T1 and T2 among the testers were identified as good general combiners indicating their ability in transmitting additive genes in the desirable direction to their progenies. Highly significant sca effects were observed in most of the hybrids for all the characters studied and good specific combiners for different characters involved parents with high × high, high × low, low × high and low × low general combinations.Keywords
Combining Ability, Upland Cotton, Span Length, Fibre Strength- RP-HPLC Method Development and Validation for Estimation of Sofosbuvir in Pure and Tablet Dosage Form
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Authors
Affiliations
1 Nalanda College of Pharmacy, Charlapally, Nalgonda, Telangana, IN
1 Nalanda College of Pharmacy, Charlapally, Nalgonda, Telangana, IN
Source
Asian Journal of Pharmacy and Technology, Vol 7, No 3 (2017), Pagination: 153-156Abstract
A rapid and precise Reverse Phase High Performance Liquid Chromatographic method has been developed for the validation of Sofosbuvir, in its pure form as well as in tablet dosage form. Chromatography was carried out on a Hypersil C18 (4.6×150mm, 5μ) column using a mixture of Methanol (100% v/v) as the mobile phase at a flow rate of 1.0 mL/min, the detection was carried out at 265 nm. The retention time of the Sofosbuvir was 3.515 ±0.02min. The method produce linear responses in the concentration range of 20-100μg/mL of Sofosbuvir. The method precision for the determination of assay was below 2.0% RSD. The method is useful in the quality control of bulk and pharmaceutical formulations.Keywords
Sofosbuvir, RP-HPLC, Validation, Tablet Dosage Forms.References
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- Formulation and Evaluation of Effervescent Floating Tablets of Procainamide
Abstract Views :346 |
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Authors
Affiliations
1 Department of Pharmaceutics, Mother Teresa Pharmacy College, Sathupally, Khammam Dist, 507303, IN
1 Department of Pharmaceutics, Mother Teresa Pharmacy College, Sathupally, Khammam Dist, 507303, IN
Source
Research Journal of Pharmaceutical Dosage Form and Technology, Vol 9, No 4 (2017), Pagination: 158-162Abstract
The aim of the present study was to develop floating formulation of Procainamide to maintain constant therapeutic levels of the drug for over 10 hrs. Various eudragit polymers were employed as polymers. Procainamide dose was fixed as 20 mg. Total weight of the tablet was considered as 300 mg. Polymers were used in the concentration of 30,60 and 90 mg concentration. All the formulations were passed various physicochemical evaluation parameters and they were found to be within limits. Whereas from the dissolution studies it was evident that the formulation (F2) showed better and desired drug release pattern i.e., 99.4 % in 12 hours. It contains the eudragit polymer Procainamide as sustained release material. It followed zero order release kinetics mechanism.Keywords
Procainamide, Eudragit (L 100, S 100, RSPO) Floating Tablets.References
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- M. Ehsanul H. Chowdhury*, M. S. I. Pathan Preparation and evaluation of floating matrix tablets of Ranitidine Hydrochloride The Pharma Innovation ISSN: 2277- 7695 Vol. 1 No. 7 2012 Online Available at www.thepharmajournal.com
- Farnaz Fouladi and Seyed Alireza Mortazavi paration and Invitro Evaluation of Gastroretentive Bupropion Hydrochloride Tablets Tropical Journal of Pharmaceutical Research June 2012; 11 (3): 351-359 http://www.tjpr.org
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- Abeda Aqther, B. Pragati kumar, Peer Basha Formulation And In-Vitro Evaluation Of Ornidazole Gastroretentive Tablets By Using Low Density Swellable Polymers ndian Journal of Research in Pharmacy and Biotechnology ISSN: 23215674(Print) ISSN: 2320 – 3471 www.ijrpb.com
- N. G. Raghavendra Rao , Harsh A Panchal1 and Pentewar Ram Formulation and in-vitro evaluation gastroretentive drug delivery system of Cefixime for prolong release Pelagia Research Library Der Pharmacia Sinica, 2011, 2 (2): 236-248
- Abbaraju Prasanna Lakshmi*, Giddam Ashwini Kumar, T. Karnaker Reddy, M. Anand Kumar Development And Invitro Evaluation of Gastroretentive Verapamil Hcl Floating Tablets International Journal of Pharmacy and Pharmaceutical Sciences ISSN- 0975-1491 Vol 4, Issue 1, 2012 360-363
- Ritesh Kumar , Amrish Chandra , Seema Garg Formulation And In Vitro Evaluation Of Sustained Release Gastroretentive Tablets Of Metformin Hydrochloride International Journal of Therapeutic Applications, Volume 7, 2012, 13 -17
- R. Narayana Charyulu, Amit B. Patil, Lakshmi Deepika C. H, Prabhakar Prabhu, Shastry C.S Development of Gastro Retentive Floating Matrix Tablets of Diltiazem Hydrochloride NUJHS Vol. I, No.1-3, September 2011
- N. G. Raghavendra Rao , Harsh A Panchal1 and Pentewar Ram Formulation and in-vitro evaluation gastroretentive drug delivery system of Cefixime for prolong release Pelagia Research Library Der Pharmacia Sinica, 2011, 2 (2): 236-248
- Yash Paul, Manoj Kumar and Bhupinder Singh Formulation and in Vitro evaluation of Gastroretentive drug delivery system of Cefixime Trihydrate International Journal of Drug Development and Research| October-December 2011 | Vol. 3 | Issue 4 | ISSN 0975-9344 | Available online http://www.ijddr.in 148-161
- K. Viveksarathi, K. Kannan, S. Selvamuthu Kumar, R. Manavalan Formulation Development and In-Vitro Evaluation of Gastroretentive Floating tablets of Atenolol J. Pharm. Sci. and Res. Vol.3(12), 2011,1632-1636
- Jadhav Mayur N., S. Shanmugam, K. Sundaramoorthy, T. Ayyappan And T. Vetrichelvan. Formulation And In-Vitro Evaluation of Gastro Retentive Floating Matrix Tablets of Famotidine International Journal of Pharma and Bio Sciences ISSN 0975-6299 Vol.1/Issue-4/Oct-Dec.2010 www.ijpbs.net
- Farnaz Fouladi and Seyed Alireza Mortazavi paration and Invitro Evaluation of Gastroretentive Bupropion Hydrochloride Tablets Tropical Journal of Pharmaceutical Research June 2012; 11 (3): 351-359 http://www.tjpr.org
- Basawaraj S. Patil, Sandeep J. Sonawane, Upendra Kulkarni, Hariprasanna R. C. Formulation and in-vitro Evaluation of Captopril Floating Matrix Tablets Using HPMC 50cps JPSBR: Volume 2, Issue 3: May Jun 2012 (97-102) ISSN NO. 2271-3681