Pharmaceutics PYQs – Set 109
Subject : Pharmaceutics
2161. pH of 0.005M HCl is:
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2162. Sugar in protein preparation acts as:
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2163. Polymethyl methacrylate (PMMA) is known as
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2164. Zydis, oral disintegrating tablet, is produced by lyophilizing or freeze-drying the drug in a matrix, usually of
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2165. WITEPSOL is a trade name of
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2166. Which of the following properties is NOT a characteristic of microemulsions
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2167. What would be the drug plasma concentration immediately after an intravenous dose of 2 m with volume of distribution (VD) of 20L is given to a 65-kg male patient? (VD = dose/CP0)
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2168. The highest dustability is observed for
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2169. Reynold's number is defined as the ratio of inertia force to
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2170. A typical hard capsule gelatin type A specification with respect to pH is :
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2171. VIVASOL® is
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2172. Reasons for capping in tablet formulations are all EXCEPT
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2173. At pH 5.0, the ratio of the protonated to unprotonated forms of morphine (a weak base containing an ionizable amine group, pKa = 7.0) would be
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2174. Class IV drug
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2175. Starting material for synthesis of polyvinylalcohol is
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2176. ––––– is enteric tablet coating material
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2177. Craig apparatus is used in experiments for
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2178. If the Zeta potential of a colloidal dispersion is 0 to ±5 mV, that colloid shows
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2179. Beta-lactam antibiotics are most likely to degrade as a result of
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2180. According to Higuchi model, drug release from porous matrix is directly related to
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