1 1. Define Suppositories and pessaries, Displacement value and evaluation. Define different extraction processes like infusion, Decoction, Maceration and Percolation 2. Pharmaceutical calculations, Define Surgical dressings, absorbable gelatin sponge, sutures, Classification of Incompatibilities DPH-102: Pharmaceutics 2 1. Discuss amino acid & nucleic acid derivatives 2. Explain LFT, KFT and Electrolytes in detail Med Biochem in eASY AND SHORT EXAMINATION

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DPH-102: PHARMACEUTICS


PAPER 1 - SECTION 1


1. Suppositories and Pessaries

Definition: Suppositories are solid dosage forms meant for insertion into body orifices other than the mouth (rectum, vagina, urethra). They melt, dissolve, or soften at body temperature to release the drug.
Types by route:
  • Rectal suppositories - torpedo/bullet shaped, ~2g (adults), ~1g (children)
  • Vaginal suppositories (pessaries) - ovoid/globular, ~5g
  • Urethral suppositories (bougies) - pencil-shaped, ~4g
Pessaries: Solid dosage forms specifically designed for vaginal administration. Used for local action (antifungals, antibiotics, contraceptives, estrogens).
Bases used:
TypeExample
Oleaginous (melting)Cocoa butter (theobroma oil)
Water-soluble/misciblePEG (polyethylene glycol)
EmulsifyingGlycerogelatin

2. Displacement Value (DV)

Definition: The number of parts by weight of a drug that displaces one part by weight of the base (usually cocoa butter).
Why it matters: Drugs are denser than the base. Adding drug without adjustment gives a suppository heavier than intended with incorrect dose.
Formula:
DV = Weight of drug / Weight of base displaced
Calculation example:
  • Mold capacity = 2g cocoa butter
  • DV of zinc oxide = 4.7
  • For 0.5g zinc oxide per suppository:
    • Base displaced = 0.5 / 4.7 = 0.106g
    • Cocoa butter required = 2 - 0.106 = 1.894g

3. Evaluation of Suppositories

TestPurpose
Melting/Softening pointShould melt at 36-37°C (body temp); use melting point apparatus
Liquefaction timeTime to liquefy in water bath at 37°C; should be < 30 min
Dissolution testFor water-soluble bases
Breaking testMechanical strength; should withstand handling
Weight variationNot more than ±5% deviation from mean
Drug content uniformityChemical assay for active ingredient
Leakage testWrapped in foil, placed at 37°C; no leakage allowed

4. Extraction Processes

a) Infusion

  • Definition: Prepared by pouring boiling (or cold) water over crude drug and allowing to stand.
  • Hot infusion: Drug + boiling water, steeped for 15 minutes, strained.
  • Cold infusion: Drug soaked in cold water for several hours.
  • Used for: Delicate plant parts - leaves, flowers, aromatic herbs.
  • Example: Ginger infusion, chamomile tea.
  • Shelf life: Short (prepared fresh daily).

b) Decoction

  • Definition: Prepared by boiling crude drug with water for a definite time (usually 15-20 minutes), then straining.
  • Used for: Hard, woody plant parts - bark, roots, rhizomes, seeds.
  • Example: Senna decoction, cinnamon decoction.
  • Difference from infusion: Heat is applied throughout (boiled, not just steeped).

c) Maceration

  • Definition: Drug is soaked in solvent (menstruum) at room temperature for a specified period (usually 2-7 days) with occasional agitation, then strained and marc pressed.
  • Solvent: Water, alcohol, or hydroalcoholic mixture.
  • Used for: Drugs whose constituents are soluble in cold solvent; drugs damaged by heat.
  • Example: Garlic maceration, belladonna tincture.
  • Advantage: Simple; suitable for thermo-labile drugs.
  • Disadvantage: Slow; incomplete extraction.

d) Percolation

  • Definition: Solvent (menstruum) is allowed to pass slowly downward through a column of powdered drug in a cone-shaped vessel (percolator). Fresh solvent continuously contacts drug, giving complete extraction.
  • Steps: Moistening drug → packing in percolator → allowing maceration → collecting percolate.
  • Used for: Large-scale preparation; most tinctures and fluid extracts.
  • Advantage: Complete, efficient extraction.
  • Example: Nux vomica tincture.
MethodTemperatureTimeBest For
InfusionHot/Cold15 minDelicate parts
DecoctionBoiling15-20 minHard parts
MacerationRoom temp2-7 daysThermo-labile
PercolationRoom tempHours-daysLarge scale/tinctures

PAPER 1 - SECTION 2


5. Pharmaceutical Calculations (Key Concepts)

Percentage calculations:
  • % w/w = grams of solute per 100g solution
  • % w/v = grams of solute per 100mL solution
  • % v/v = mL of solute per 100mL solution
Dilution formula: C1V1 = C2V2
Doses:
  • Child's dose (Young's formula): (Age / Age+12) × Adult dose
  • Clark's formula: (Weight in lbs / 150) × Adult dose
Proof spirit: 100 proof = 50% v/v ethanol

6. Surgical Dressings

Definition: Materials used to cover, protect, and aid healing of wounds, burns, and surgical incisions.
Ideal properties: Sterile, non-toxic, non-irritant, absorbent, non-adherent to wound, comfortable, permeable to air.
Types:
TypeDescription
Absorbent cottonPurified cellulose fiber; highly absorbent
GauzeLoosely woven cotton fabric
BandagesRoller bandages (cotton/elastic)
Adhesive plastersCotton/synthetic fabric with adhesive
Paraffin gauzeGauze impregnated with soft paraffin (non-adherent)

7. Absorbable Gelatin Sponge

  • Definition: A sterile, absorbable, water-insoluble, off-white, non-elastic porous sponge made from purified gelatin solution.
  • Properties: Completely absorbed by body tissues in 4-6 weeks; can absorb 40 times its weight in blood.
  • Uses:
    • Hemostasis during surgical procedures
    • Control of capillary bleeding
    • Packing dental sockets after extraction
    • Neurosurgery and ENT surgery
  • Mechanism: Provides scaffold for clot formation; swells and mechanically stops bleeding.
  • Brand name: Gelfoam

8. Sutures

Definition: Sterile strands used to close wounds, ligate blood vessels, and approximate tissue layers.
Classification:
A. By Absorbability:
AbsorbableNon-absorbable
Catgut (plain/chromic)Silk
Polyglycolic acid (Dexon)Nylon (Prolene)
Polyglactin (Vicryl)Polypropylene
Polyglecaprone (Monocryl)Steel wire
B. By Origin:
  • Natural: Catgut, silk, cotton, linen
  • Synthetic: Nylon, Dacron, Vicryl, PDS
C. By Structure:
  • Monofilament: Single strand (Nylon, Prolene) - less bacterial adherence
  • Multifilament/Braided: Multiple strands twisted (Silk, Vicryl) - easier to handle
Needle types: Cutting (skin), Round-bodied (soft tissue), Taper-cut (tough tissue)

9. Classification of Incompatibilities

Definition: Incompatibility occurs when two or more substances in a prescription react together to produce an undesirable change in physical appearance, chemical nature, or therapeutic activity.

A. Physical Incompatibility

Physical change without chemical reaction.
  • Immiscibility: Mixing of two immiscible liquids (oil + water)
  • Liquefaction of solids: Eutectic mixtures (e.g., menthol + camphor)
  • Insolubility/precipitation: Adding alcohol-soluble drug to water
  • Color change: Physical adsorption

B. Chemical Incompatibility

New chemical compound formed.
  • Oxidation-reduction: e.g., potassium permanganate + glycerin (explosion risk)
  • Double decomposition/precipitation: e.g., lead acetate + sodium sulfate → lead sulfate (precipitate)
  • Hydrolysis: e.g., aspirin + water → salicylic acid + acetic acid
  • Complexation: Tetracycline + calcium/antacids → chelation

C. Therapeutic Incompatibility

Undesirable therapeutic outcome.
  • Synergism (adverse): Two CNS depressants → excess sedation
  • Antagonism: Heparin + protamine sulfate (desired antidote, but incompatible if overdosed)
  • Potentiation: e.g., sulfonamides + trimethoprim potentiation (desired but can cause toxicity)


MED BIOCHEMISTRY - PAPER 2


SECTION 1: Amino Acid & Nucleic Acid Derivatives


1. Amino Acid Derivatives

Amino acids are not just building blocks of proteins; they are precursors to many biologically active molecules.

Key Derivatives:

Amino AcidDerivativeFunction
TyrosineDopamine, Norepinephrine, EpinephrineCatecholamine neurotransmitters
TyrosineThyroid hormones (T3, T4)Metabolic regulation
TyrosineMelaninSkin/hair pigment
TryptophanSerotonin (5-HT)Mood, sleep, GI motility
TryptophanMelatoninCircadian rhythm
TryptophanNiacin (Vit B3)NAD+/NADP+ synthesis
HistidineHistamineAllergic response, gastric acid secretion
GlutamateGABAInhibitory neurotransmitter
GlycineHeme (with succinyl CoA)Oxygen transport
GlycineCreatineMuscle energy (PCr)
ArginineNitric oxide (NO)Vasodilation
PhenylalaninePhenylethylamine; also → TyrosineNeuromodulator
SerineEthanolamine → Choline → AcetylcholineNeurotransmitter
CysteineGlutathione (GSH)Antioxidant

2. Nucleic Acid Derivatives

Nucleotides are derivatives of purine and pyrimidine bases + sugar + phosphate.

Purine bases: Adenine, Guanine

Pyrimidine bases: Cytosine, Thymine (DNA), Uracil (RNA)

Important Nucleotide Derivatives:

DerivativeFunction
ATP (Adenosine triphosphate)Universal energy currency
AMP/cAMPSecond messenger (protein kinase A activation)
cGMPSecond messenger (NO pathway)
NAD+/NADHElectron carriers in cellular respiration
NADP+/NADPHReductive biosynthesis (fatty acid, steroid synthesis)
FAD/FADH2Electron carriers (Complex II of ETC)
CoA (Coenzyme A)Acyl group carrier; key in Krebs cycle
SAM (S-Adenosylmethionine)Universal methyl group donor
GTPEnergy in protein synthesis, signal transduction

SECTION 2: LFT, KFT and Electrolytes


Liver Function Tests (LFT)

Tests used to assess hepatocellular damage, synthetic function, and biliary obstruction.
TestNormal RangeSignificance
Bilirubin (Total)0.2-1.2 mg/dLElevated in jaundice
Direct (conjugated) bilirubin0-0.3 mg/dLElevated in obstructive/hepatic jaundice
Indirect (unconjugated)0.2-0.8 mg/dLElevated in hemolytic jaundice
AST (SGOT)10-40 U/LHepatocellular damage, MI
ALT (SGPT)7-56 U/LMore specific to liver
ALP (Alkaline phosphatase)44-147 U/LBiliary obstruction, bone disease
GGT9-48 U/LAlcohol liver disease, cholestasis
Total protein6-8 g/dLSynthetic function
Albumin3.5-5 g/dLChronic liver disease if low
PT/INRINR 0.9-1.1Coagulation factor synthesis
Pattern recognition:
  • Hepatocellular: AST/ALT elevated predominantly
  • Cholestatic: ALP/GGT elevated predominantly
  • Synthetic failure: Low albumin, prolonged PT

Kidney Function Tests (KFT)

TestNormal RangeSignificance
Serum CreatinineM: 0.7-1.3 mg/dL; F: 0.6-1.1 mg/dLBest single marker of GFR
Blood Urea Nitrogen (BUN)7-20 mg/dLAffected by protein intake, dehydration
BUN:Creatinine ratio10:1-20:1>20: prerenal; <10: renal/postrenal
GFR (eGFR)>90 mL/min/1.73m²CKD stages by GFR
Uric acidM: 3.5-7.2 mg/dL; F: 2.6-6 mg/dLElevated in gout, renal failure
24h urine creatinine500-2000 mg/dayCreatinine clearance
Urine protein< 150 mg/dayProteinuria indicates renal damage
CKD Staging by eGFR:
  • Stage 1: ≥90 (with kidney damage markers)
  • Stage 2: 60-89
  • Stage 3a: 45-59
  • Stage 3b: 30-44
  • Stage 4: 15-29
  • Stage 5: <15 (Kidney failure)

Electrolytes

Sodium (Na+)

  • Normal: 135-145 mEq/L
  • Hyponatremia (<135): Confusion, seizures; causes: SIADH, heart failure, liver cirrhosis
  • Hypernatremia (>145): Thirst, dehydration, altered sensorium; causes: Diabetes insipidus, excess sodium intake

Potassium (K+)

  • Normal: 3.5-5.0 mEq/L
  • Hypokalemia (<3.5): Muscle weakness, U-wave on ECG, arrhythmias; causes: diuretics, vomiting, diarrhea
  • Hyperkalemia (>5.0): Peaked T-waves, fatal arrhythmias; causes: renal failure, ACE inhibitors, Addison's disease

Calcium (Ca2+)

  • Normal: 8.5-10.5 mg/dL (total); ionized: 4.5-5.5 mg/dL
  • Hypocalcemia: Tetany, Chvostek's/Trousseau's sign, prolonged QT
  • Hypercalcemia: "Bones, Stones, Groans, Moans" (hyperparathyroidism, malignancy)

Bicarbonate (HCO3-)

  • Normal: 22-26 mEq/L
  • Low: Metabolic acidosis
  • High: Metabolic alkalosis

Chloride (Cl-)

  • Normal: 98-106 mEq/L
  • Used in anion gap calculation: AG = Na - (Cl + HCO3); Normal = 8-12

Phosphate (PO4)

  • Normal: 2.5-4.5 mg/dL
  • Low in hyperparathyroidism, rickets
  • High in renal failure, hypoparathyroidism

Quick Exam Tips:
  • For LFT: Remember ALT is more liver-specific than AST
  • For KFT: Creatinine is the best GFR marker (BUN is unreliable alone)
  • Electrolytes: Always link to ECG changes for K+ and Ca2+
  • Displacement value: DV = Weight of drug / Weight of base displaced
  • Percolation = most efficient extraction; Infusion = quickest
  • Incompatibilities: Physical = appearance change; Chemical = new compound; Therapeutic = altered drug effect
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