| Term 
 
        | What are 2 Physicochemical Parameters? |  | Definition 
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        | Term 
 
        | What are 3 Physicochemical Parameters of Drugs? |  | Definition 
 
        | •	Hydrophilic Drugs •	Hydrophobic Drugs
 •	Weak Acid or Weak Base
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        | Term 
 
        | Describe rate of release for Hydrophilic Drugs and what they are used for |  | Definition 
 
        | –	Rapid rate of release –	Used for more immediate release
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        | Term 
 
        | Describe rate of release for Hydrophobic Drugs and what they are used for |  | Definition 
 
        | –	Delayed release –	Used for extended release or depot preparations
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        | Term 
 
        | What do Weak Acid or Weak Bases affect? |  | Definition 
 
        | –	Affects rate of release at site of absorption |  | 
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        | Term 
 
        | What are the 2 sub categories of Physicochemical Parameters of Dosage Form? |  | Definition 
 
        | •	Type of Delivery System •	Excipients Used
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        | Term 
 
        | What are the types of Delivery Systems? |  | Definition 
 
        | –	Immediate release or Extended Release –	Transdermal, oral
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        | Term 
 | Definition 
 
        | –	Disintegrants –	Fillers
 –	Lubricants
 –	Polymers
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        | Term 
 
        | For the Role of Excipients disintegrating agents are generally used to promote ________ of oral solid dosage forms in order to release the ________   ___________ |  | Definition 
 
        | disintegration, active ingredients |  | 
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        | Term 
 
        | For the Role of Excipients Diluents play a very important role in tablet  ________, _________, _________  and biopharmaceutical properties of tablets. |  | Definition 
 
        | hardness, disintegration, dissolution |  | 
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        | Term 
 
        | Under the same _______ force, tablets made of a same active ingredient but with different diluents have _______  ________ |  | Definition 
 
        | Compressional, different hardness. |  | 
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        | Term 
 
        | If the same tablets were made by different starches, the dissolution rate profile is .... |  | Definition 
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        | Term 
 
        | Hardness of a tablet varies based on the ... |  | Definition 
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        | Term 
 
        | Disintegration time of a tablet varies based on the ... |  | Definition 
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        | Term 
 
        | Lubricants such as magnesium stearate ______the dissolution of drug |  | Definition 
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        | Term 
 
        | Polymers used in preparation of matrix based systems change the release profile of drugs based on ... |  | Definition 
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        | Term 
 
        | Hydrophilic polymers are used for ... |  | Definition 
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        | Term 
 
        | hydrophobic are used for ... |  | Definition 
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        | Term 
 
        | Polymers used in coating process also change ... |  | Definition 
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        | Term 
 
        | Film coating polymers _____ the release of a drug for extended periods of time |  | Definition 
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        | Term 
 
        | Presence of food in the stomach can______ the release of drug |  | Definition 
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        | Term 
 
        | Enteric coated tablets release the contents only at the pH of the ... |  | Definition 
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        | Term 
 
        | pH sensitive liposomes undergo a pH induced fusion with _________  _________and directly release the liposomal content to the ________ |  | Definition 
 
        | endosomal membrane , cytosol |  | 
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        | Term 
 
        | These liposomes are stable at physiological pH and undergo degradation or deformation at _____ pH. |  | Definition 
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