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11. [Chemical changes due to the compounding of parenteral injections. (1)]. Kosugi T Iryo; 1967 Aug; 21(8):960-1. PubMed ID: 5582998 [No Abstract] [Full Text] [Related]
12. Assessment of the feasibility of oral controlled release in an exploratory development setting. Thombre AG Drug Discov Today; 2005 Sep; 10(17):1159-66. PubMed ID: 16182208 [TBL] [Abstract][Full Text] [Related]
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14. The availability of antibiotics in combination with other additives in intravenous solutions. Dancey JW; Carew DP Am J Hosp Pharm; 1966 Oct; 23(10):543-51. PubMed ID: 5915776 [No Abstract] [Full Text] [Related]
15. [Biopharmaceutical aspects of pharmaceutical technology]. Thoma K Pharmazie; 1981 Mar; 36(3):185-93. PubMed ID: 7279982 [No Abstract] [Full Text] [Related]
16. The Resotest Apparatus. A universally applicable biopharmaceutical experimental tool. Koch HP Methods Find Exp Clin Pharmacol; 1980 Apr; 2(2):97-102. PubMed ID: 7339334 [No Abstract] [Full Text] [Related]
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18. Solid lipid nanoparticles for parenteral drug delivery. Wissing SA; Kayser O; Müller RH Adv Drug Deliv Rev; 2004 May; 56(9):1257-72. PubMed ID: 15109768 [TBL] [Abstract][Full Text] [Related]
19. Nanosizing--oral formulation development and biopharmaceutical evaluation. Kesisoglou F; Panmai S; Wu Y Adv Drug Deliv Rev; 2007 Jul; 59(7):631-44. PubMed ID: 17601629 [TBL] [Abstract][Full Text] [Related]
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