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Journal Abstract Search
115 related items for PubMed ID: 3921688
1. Crystallization of excipients in tablets. Ando H, Watanabe S, Ohwaki T, Miyake Y. J Pharm Sci; 1985 Feb; 74(2):128-31. PubMed ID: 3921688 [Abstract] [Full Text] [Related]
2. Conductivity and hardness changes in aged compacts. Bhatia RP, Lordi NG. J Pharm Sci; 1979 Jul; 68(7):896-9. PubMed ID: 458612 [Abstract] [Full Text] [Related]
3. Crystal growth formation in melt extrudates. Bruce C, Fegely KA, Rajabi-Siahboomi AR, McGinity JW. Int J Pharm; 2007 Aug 16; 341(1-2):162-72. PubMed ID: 17524578 [Abstract] [Full Text] [Related]
4. Relative Humidity Cycling: Implications on the Stability of Moisture-Sensitive Drugs in Solid Pharmaceutical Products. Veronica N, Heng PWS, Liew CV. Mol Pharm; 2023 Feb 06; 20(2):1072-1085. PubMed ID: 36480246 [Abstract] [Full Text] [Related]
5. Differential scanning calorimetry to investigate the compatibility of ciprofloxacin hydrochloride with excipients. Fathy M, Hassan MA, Mohamed FA. Pharmazie; 2002 Dec 06; 57(12):825-8. PubMed ID: 12561245 [Abstract] [Full Text] [Related]
6. Inhibition of the spontaneous polymorphic transition of pyrazinamide γ form at room temperature by co-spray drying with 1,3-dimethylurea. Baaklini G, Dupray V, Coquerel G. Int J Pharm; 2015 Feb 01; 479(1):163-70. PubMed ID: 25556055 [Abstract] [Full Text] [Related]
8. Investigation of physicochemical factors affecting the stability of a pH-modulated solid dispersion and a tablet during storage. Tran PH, Tran TT, Park JB, Min DH, Choi HG, Han HK, Rhee YS, Lee BJ. Int J Pharm; 2011 Jul 29; 414(1-2):48-55. PubMed ID: 21565260 [Abstract] [Full Text] [Related]
9. Physicochemical stability of crystalline sugars and their spray-dried forms: dependence upon relative humidity and suitability for use in powder inhalers. Naini V, Byron PR, Phillips EM. Drug Dev Ind Pharm; 1998 Oct 29; 24(10):895-909. PubMed ID: 9876544 [Abstract] [Full Text] [Related]
10. Influence of excipients in comilling on mitigating milling-induced amorphization or structural disorder of crystalline pharmaceutical actives. Balani PN, Ng WK, Tan RB, Chan SY. J Pharm Sci; 2010 May 29; 99(5):2462-74. PubMed ID: 19902526 [Abstract] [Full Text] [Related]
14. Application of differential scanning calorimetry in evaluation of solid state interactions in tablets containing acetaminophen. Mazurek-Wadołkowska E, Winnicka K, Czajkowska-Kośnik A, Czyzewska U, Miltyk W. Acta Pol Pharm; 2013 May 29; 70(5):787-93. PubMed ID: 24147356 [Abstract] [Full Text] [Related]
16. Influence of protein on mannitol polymorphic form produced during co-spray drying. Hulse WL, Forbes RT, Bonner MC, Getrost M. Int J Pharm; 2009 Dec 01; 382(1-2):67-72. PubMed ID: 19682563 [Abstract] [Full Text] [Related]
17. Comparative evaluation of two direct compression lactose grades for pyridoxine hydrochloride tablets. Aly SA, Udeala OK. Pharmazie; 1988 Mar 01; 43(3):188-90. PubMed ID: 3380861 [Abstract] [Full Text] [Related]
18. Development of manufacturing method for rapidly disintegrating oral tablets using the crystalline transition of amorphous sucrose. Sugimoto M, Narisawa S, Matsubara K, Yoshino H, Nakano M, Handa T. Int J Pharm; 2006 Aug 31; 320(1-2):71-8. PubMed ID: 16750604 [Abstract] [Full Text] [Related]
19. The effect of excipients on the stability of levothyroxine sodium pentahydrate tablets. Patel H, Stalcup A, Dansereau R, Sakr A. Int J Pharm; 2003 Oct 02; 264(1-2):35-43. PubMed ID: 12972334 [Abstract] [Full Text] [Related]