Growup Pharma

B Pharmacy Sem 2: Remedial Biology / Mathematics

B Pharmacy Sem 2: Remedial Biology / Mathematics

 

Table of Contents

Subject : Remedial Biology / Mathematics (as applicable)


1.  If Remedial Biology:

  1. Cell Biology & Biomolecules
  2. Basic Genetics & Human Organ Systems Review
  3. Plant Anatomy & Physiology
  4. Microbiology Fundamentals

2.  If Remedial Mathematics:

  1. Algebraic Expressions & Logarithms
  2. Differentiation & Integration Basics
  3. Elementary Statistics (Mean, Median, Mode)
  4. Pharmaceutical Calculations Review

 

Lets See first the Remedial Biology:

 

Unit 1: Cell Biology & Biomolecules

This unit introduces the fundamental structural and functional aspects of the cell and the chemical building blocks (biomolecules) that underpin all cellular processes.


1.1 Cell Theory & Cell Types

  • Cell Theory:

    1. All living organisms are composed of one or more cells.

    2. The cell is the basic unit of life.

    3. All cells arise from pre‑existing cells.

  • Prokaryotic vs. Eukaryotic Cells:

    FeatureProkaryoteEukaryote
    NucleusAbsent; DNA in nucleoidTrue nucleus with nuclear envelope
    OrganellesFew membrane‑bound (ribosomes)Numerous (mitochondria, ER, Golgi, etc.)
    Size0.1–5 µm10–100 µm
    ExamplesBacteria, ArchaeaAnimal, plant, fungal, protist cells

1.2 Cell Membrane & Transport Mechanisms

  • Fluid Mosaic Model: phospholipid bilayer with embedded proteins, cholesterol, glycoproteins.

  • Membrane Functions: barrier, signal transduction, cell recognition, transport.

  • Transport Processes:

    • Passive:

      • Simple diffusion (small non‑polar molecules)

      • Facilitated diffusion (via channels/carriers)

      • Osmosis (water through aquaporins)

    • Active:

      • Primary active transport (e.g., Na⁺/K⁺‑ATPase)

      • Secondary active transport (symporters/antiporters)

    • Vesicular: endocytosis (phagocytosis, pinocytosis), exocytosis.


1.3 Membrane‑Bound Organelles & Their Roles

OrganelleStructure & Function
NucleusDNA storage; transcription; nuclear pores for traffic
Endoplasmic ReticulumRough ER: protein synthesis; Smooth ER: lipid synthesis, detoxification
Golgi ApparatusProtein/glycoprotein modification, sorting, packaging
MitochondriaATP production via oxidative phosphorylation; apoptosis regulation
LysosomesDigestive enzymes degrade macromolecules, organelles
Peroxisomesβ‑oxidation of fatty acids; detoxify H₂O₂ via catalase

1.4 Cytoskeleton & Cell Division Overview

  • Cytoskeleton:

    • Microfilaments (actin): cell shape, movement, cytokinesis

    • Microtubules (tubulin): vesicle transport, mitotic spindle

    • Intermediate Filaments: mechanical support

  • Cell Cycle Phases:

    • G₁ (growth), S (DNA replication), G₂ (preparation), M (mitosis)

    • Checkpoints: G₁/S, G₂/M ensure genomic integrity


1.5 Biomolecules: Building Blocks of the Cell

1.5.1 Carbohydrates

  • Monosaccharides (glucose, fructose), disaccharides (sucrose), polysaccharides (glycogen, cellulose).

  • Functions: energy source (glycolysis), structural (cell wall), cell recognition (glycocalyx).

1.5.2 Lipids

  • Neutral lipids: triglycerides for energy storage

  • Phospholipids & glycolipids: membrane structure

  • Steroids: cholesterol (membrane fluidity), precursors for steroid hormones

  • Function: energy, insulation, membrane integrity, signaling (eicosanoids).

1.5.3 Proteins

  • Amino acids linked by peptide bonds.

  • Levels of structure: primary → secondary (α‑helix, β‑sheet) → tertiary → quaternary.

  • Functions: enzymes (catalysis), transport (hemoglobin), signaling (receptors), structural (collagen).

1.5.4 Nucleic Acids

  • DNA: deoxyribonucleotides store genetic information in double helix.

  • RNA: ribonucleotides (mRNA, tRNA, rRNA) mediate gene expression.

  • Functions: replication, transcription, translation.


1.6 Clinical & Pharmaceutical Relevance

  • Membrane Transporters as drug targets (e.g., P‑gp efflux pumps affecting bioavailability).

  • Enzymes in drug metabolism (e.g., cytochrome P450 in ER).

  • Mitochondrial toxicity: some drugs disrupt oxidative phosphorylation (e.g., certain antivirals).

  • Biomolecule assays: quantification of proteins (Bradford), nucleic acids (UV absorbance) in QC.


1.7 Key Points for Exams

  • State the cell theory and distinguish prokaryotes from eukaryotes.

  • Describe the fluid mosaic model and list transport mechanisms.

  • Match major organelles to their functions.

  • Outline the cytoskeletal components and cell cycle phases.

  • Identify the four classes of biomolecules, their subunits, and primary roles.

 

 

Unit 2: Basic Genetics & Human Organ Systems Review

This unit provides a foundational understanding of genetic principles relevant to pharmacy (drug response, pharmacogenomics) and a concise review of major human organ systems, emphasizing their physiological functions and relevance to pharmacotherapy.


2.1 Introduction to Genetics in Pharmacy

2.1.1 DNA Structure & Function

  • Double Helix: two antiparallel strands of deoxyribonucleotides (A–T, G–C base pairing).

  • Genes: DNA segments encoding proteins or functional RNA.

  • Chromosomes: organized DNA–protein complexes; humans have 23 pairs.

2.1.2 Gene Expression

  1. Transcription: DNA → pre‑mRNA in nucleus (RNA polymerase II).

  2. RNA Processing: 5′ cap, poly‑A tail, splicing of introns → mature mRNA.

  3. Translation: mRNA → polypeptide at ribosomes; tRNA delivers amino acids.

2.1.3 Genetic Variation & Pharmacogenomics

  • Polymorphisms: single nucleotide polymorphisms (SNPs) can alter drug‑metabolizing enzymes (e.g., CYP450 variants), transporters, or receptors.

  • Examples:

    • CYP2D6 Poor Metabolizers: risk of toxicity with codeine (reduced conversion to morphine).

    • TPMT Deficiency: high risk of myelosuppression with thiopurines.

  • Clinical Application: genotype‑guided dosing improves safety and efficacy.


2.2 Mendelian Genetics

PrincipleDescription
Law of SegregationTwo alleles of a gene segregate during gamete formation; each gamete carries one allele.
Law of Independent AssortmentGenes for different traits assort independently if on different chromosomes.
Dominant & RecessiveDominant allele expresses phenotype in heterozygote; recessive requires homozygosity.
Genotype vs. PhenotypeGenotype = genetic makeup; phenotype = observable trait influenced by genotype and environment.

2.2.1 Punnett Squares & Inheritance Patterns

  • Autosomal Dominant: one mutant allele causes disease (e.g., familial hypercholesterolemia).

  • Autosomal Recessive: two mutant alleles required (e.g., cystic fibrosis).

  • X‑Linked: mutation on X chromosome (e.g., hemophilia A).


2.3 Human Organ Systems Overview

SystemMajor FunctionsPharmacological Relevance
CardiovascularPumping blood, nutrient/gas transport, pressure regulationAntihypertensives, antiarrhythmics, anticoagulants
RespiratoryGas exchange (O₂/CO₂), acid–base balanceBronchodilators, steroids, antibiotics for pneumonia
DigestiveIngestion, digestion, absorption, waste eliminationProton‑pump inhibitors, antiemetics, antidiarrheals
NervousSensory input, processing, motor outputAnalgesics, antiepileptics, psychotropics
EndocrineHormone secretion for metabolism, growth, reproductionInsulin, thyroid hormones, corticosteroids
Renal/UrinaryFiltration, excretion, fluid/electrolyte balanceDiuretics, ACE inhibitors, electrolyte supplements
MusculoskeletalSupport, movement, mineral storageNSAIDs, muscle relaxants, bone‑active agents (bisphosphonates)
Immune/LymphaticDefense against pathogens, fluid balanceVaccines, immunosuppressants, monoclonal antibodies
IntegumentaryProtection, temperature regulation, sensationTopical corticosteroids, antibacterials, emollients
ReproductiveGametogenesis, hormone productionHormonal contraceptives, fertility agents

2.4 Selected System Highlights

2.4.1 Cardiovascular System

  • Heart: cardiac cycle, contractility; drug targets include β‑adrenergic receptors and calcium channels.

  • Vasculature: smooth muscle tone regulated by nitric oxide, angiotensin II; antihypertensives act here.

2.4.2 Renal System

  • Nephron Function: filtration, reabsorption, secretion; diuretics target specific nephron segments (e.g., loop diuretics at ascending loop).

2.4.3 Nervous System

  • Neurotransmitters: acetylcholine, dopamine, serotonin; psychotropic drugs modulate these pathways.

  • Blood–Brain Barrier: impacts CNS drug delivery; lipophilicity and transporters are key.


2.5 Integrating Genetics and Physiology

  • Pharmacokinetics (PK): genetic variation in metabolizing enzymes affects absorption, distribution, metabolism, and excretion.

  • Pharmacodynamics (PD): receptor polymorphisms alter drug response (e.g., β₂‑adrenergic receptor variants affect asthma therapy).

  • Personalized Medicine: combining genotype data with organ‑system knowledge to tailor therapy.


2.6 Key Points for Exams

  • Describe DNA → RNA → protein central dogma and relate to drug target synthesis.

  • Explain Mendelian inheritance laws and apply Punnett squares to basic scenarios.

  • Recognize major organ systems, their primary functions, and corresponding drug classes.

  • Illustrate how pharmacogenomic variants (e.g., CYP450) influence drug metabolism and therapy.

  • Integrate genetics with physiology to understand personalized pharmacotherapy.

Unit 3: Plant Anatomy & Physiology

This unit provides a foundational overview of plant structure and function, emphasizing aspects relevant to pharmacognosy and herbal drug technology.


3.1 Plant Cell & Tissue Organization

Tissue TypeLocationCharacteristics & Functions
MeristematicShoot/root apices, cambiumUndifferentiated, actively dividing cells—growth zones
DermalEpidermisProtective outer layer; cuticle reduces water loss
GroundCortex, pithParenchyma (storage/photosynthesis), collenchyma (support), sclerenchyma (rigidity)
VascularXylem & phloem bundlesXylem transports water/minerals; phloem translocates photosynthates

3.2 Root Anatomy & Function

  • Primary Structure:

    • Epidermis with root hairs for absorption

    • Cortex of parenchyma for storage

    • Endodermis with Casparian strips regulating solute entry

    • Stele containing xylem (star‑shaped in dicots) and phloem

  • Physiological Roles:

    • Water and mineral uptake via apoplastic and symplastic routes

    • Anchoring plant and storage of carbohydrates


3.3 Stem Anatomy & Transport

  • Externally: nodes (leaf attachment) and internodes; lenticels for gas exchange in woody stems

  • Vascular Arrangement:

    • Dicots: ring of vascular bundles; cambial layer produces secondary growth

    • Monocots: scattered vascular bundles; no true secondary growth

  • Xylem Vessels & Tracheids: thick‑walled conduits for bulk water flow

  • Phloem Sieve Tubes & Companion Cells: living elements for bidirectional sugar transport (pressure‑flow mechanism)


3.4 Leaf Structure & Photosynthesis

Leaf RegionFeaturesRole
Epidermis & CuticleWaxy cuticle, stomata guard cellsMinimize water loss; gas exchange regulation
MesophyllPalisade (chloroplast‑rich) & spongy cellsLight capture and CO₂ diffusion
VeinsVascular bundlesDeliver water; export photosynthates
  • Photosynthesis (C₃ pathway):

    1. Light Reactions (thylakoid membranes): H₂O → O₂; ATP & NADPH generation

    2. Calvin Cycle (stroma): CO₂ fixation by Rubisco → triose phosphates → sucrose/starch

  • C₄ & CAM Adaptations: spatial (bundle sheath) or temporal (night fixation) separation to minimize photorespiration—important in certain medicinal plants.


3.5 Transpiration & Mineral Nutrition

  • Transpiration Stream:

    • Cohesion‑tension mechanism pulls xylem sap upward

    • Regulated by stomatal aperture (ABA hormone triggers closure under drought)

  • Essential Minerals & Uptake:

    MacronutrientFunctionDeficiency Symptom
    N (nitrate)Amino acids, chlorophyllChlorosis, stunted growth
    P (phosphate)ATP, nucleic acidsDark green leaves, delayed maturity
    K (potassium)Osmoregulation, enzyme activationMarginal chlorosis, weak stems
  • Mycorrhizae: symbiosis enhancing phosphate and water uptake—relevant in cultivation of medicinal herbs.


3.6 Secondary Metabolite Production

  • Pathways: derived from phenylpropanoid, terpene, and alkaloid biosynthesis

  • Functions: defense (phytoalexins), attraction (pigments), allelopathy

  • Pharmaceutical Relevance: source of drugs (e.g., morphine, quinine, flavonoids)


3.7 Key Points for Exams

  • Distinguish meristematic, dermal, ground, and vascular tissues.

  • Label root and stem transverse sections; explain the role of the endodermis and cambium.

  • Outline leaf anatomy and the two stages of photosynthesis.

  • Describe the cohesion‑tension theory of transpiration and factors affecting stomatal behavior.

  • List major macronutrients, their roles, and deficiency symptoms in plants.

  • Explain how secondary metabolites are synthesized and their importance in drug discovery.

Unit 4: Microbiology Fundamentals

This unit provides an essential overview of microbiological principles, focusing on microorganisms relevant to pharmacy, sterilization, and infection control.


4.1 Classification of Microorganisms

GroupCharacteristicsExamples in Pharmacy
BacteriaProkaryotic; diverse shapes (cocci, bacilli); cell walls (Gram +/–)Contaminants in sterile products; probiotics (Lactobacillus)
FungiEukaryotic; yeasts (unicellular) and molds (multicellular)Antibiotic producers (Penicillium); spoilage in oral liquids
VirusesAcellular; require host cells; DNA or RNA genomeContamination risk in biologicals; viral vectors in gene therapy
ProtozoaUnicellular eukaryotes, often motileRare in pharmaceuticals; models for drug screening
AlgaePhotosynthetic eukaryotesSources of toxins (cyanobacteria) in natural products

4.2 Microbial Cell Structure & Growth

  • Bacterial Cell Envelope:

    • Gram‑positive: thick peptidoglycan, teichoic acids; retains crystal violet.

    • Gram‑negative: thin peptidoglycan, outer membrane with lipopolysaccharide; safranin counterstain.

  • Fungal Structure: chitin cell wall; ergosterol in membrane (antifungal target).

  • Viral Structure: protein capsid, sometimes lipid envelope; classification by Baltimore system.

  • Microbial Growth Curve:

    1. Lag Phase: adaptation, no division

    2. Log (Exponential) Phase: rapid division, target for antibiotics

    3. Stationary Phase: nutrient depletion, waste accumulation

    4. Death Phase: decline in viable cells


4.3 Sterilization & Disinfection

MethodMechanismUses in Pharmacy
Moist Heat (Autoclave)Denatures proteins; steam under pressureSterile solutions, surgical instruments
Dry Heat (Oven)Oxidation and protein denaturationGlassware, metal instruments
FiltrationPhysical removal of microbes (0.22 µm filters)Heat-labile liquids, vaccines
Radiation (Gamma, UV)DNA damageSingle-use plastics, surface decontamination
Chemical SterilantsAlkylation or oxidation (e.g., ethylene oxide, glutaraldehyde)Medical devices, tubings
Alcohols & PhenolicsProtein denaturation, membrane disruptionSurface disinfection, skin antisepsis

4.4 Aseptic Techniques & Contamination Control

  • Cleanroom Classifications: ISO 5–8; controlled airflow, HEPA filtration.

  • Aseptic Practices: gowning, glove use, laminar flow hoods, minimal movement.

  • Media Preparation & Sterility Testing:

    • Culture media (e.g., nutrient agar, Sabouraud’s) for microbial enumeration.

    • Bioburden Testing: pre-sterilization microbial load.

    • Sterility Test: incubate product samples in fluid thioglycollate and soybean–casein media per pharmacopeia.


4.5 Antimicrobial Agents & Resistance

  • Antibiotics Production: fermentation organisms (e.g., Penicillium chrysogenum for penicillin).

  • Mechanisms of Action: inhibit cell wall synthesis, protein synthesis, nucleic acid synthesis, or membrane function.

  • Resistance Mechanisms: enzymatic degradation (β‑lactamases), efflux pumps, target modification.

  • Pharmacological Relevance: formulation of stable antibiotic products; stewardship to prevent resistance.


4.6 Quality Assurance in Microbiology

  • Environmental Monitoring: settle plates, active air sampling in production areas.

  • Endotoxin Testing: Limulus amebocyte lysate (LAL) for parenterals.

  • Microbial Limits: specified in pharmacopeias for nonsterile products (total aerobic count, absence of pathogens).

  • Preservative Efficacy Test: challenge tests to confirm multi-dose container safety.


4.7 Key Points for Exams

  • Differentiate sterilization vs. disinfection methods and their uses.

  • Describe the bacterial growth curve and identify the phase most susceptible to antibiotics.

  • List aseptic techniques critical for sterile manufacturing.

  • Explain antibiotic mechanisms and basic resistance strategies.

  • Recall quality control tests in pharmaceutical microbiology (sterility, bioburden, endotoxin, microbial limits).

 

Lets see the Remedial Mathematics:

 

 

Unit 1: Algebraic Expressions & Logarithms

This unit reviews manipulation of algebraic expressions and the fundamentals of logarithms, with applications to pharmaceutical contexts such as concentration calculations and pH.


1.1 Algebraic Expressions

1.1.1 Definitions

  • Variable: symbol (e.g., x, y) representing a number.

  • Constant: fixed numerical value (e.g., 5, –2).

  • Term: product of a constant and one or more variables raised to powers (e.g., 3x², –½ ab).

  • Polynomial: sum of terms with non‑negative integer exponents (e.g., 2x³ – 5x + 7).

1.1.2 Operations on Expressions

OperationRuleExample
Addition/SubtractionCombine like terms (same variables and exponents)5x² + 3x – 2x² = (5–2)x² + 3x = 3x² + 3x
MultiplicationMultiply coefficients; add exponents of like bases(2x)(3x²) = 6x³
DivisionDivide coefficients; subtract exponents(6x³)/(2x) = 3x²
ExpansionUse distributive law: a(b + c) = ab + acx(2x + 5) = 2x² + 5x
FactorizationReverse of expansion; common factor or special products (difference of squares, trinomials)x² – 9 = (x–3)(x+3); x² + 5x + 6 = (x+2)(x+3)

1.2 Practical Applications in Pharmacy

  • Formulation Equations: solving for concentrations (e.g., C₁V₁ = C₂V₂ rearranged: V₁ = C₂V₂/C₁).

  • Batch Calculations: scaling ingredient quantities proportional to batch size.

  • Rate Equations: half‑life expressions for first‑order kinetics, t½ = (0.693)/k, solved algebraically for k or t½.


1.3 Introduction to Logarithms

1.3.1 Definition

  • The logarithm base b of a number N is the exponent x to which b must be raised to yield N:

     

    logbN=xbx=N. \log_b N = x \quad\Leftrightarrow\quad b^x = N.

  • Common Logarithm: base 10 (log N).

  • Natural Logarithm: base e ≈ 2.718 (ln N).

1.3.2 Logarithm Properties

PropertyFormula
Product Rule 

logb(MN)=logbM+logbN\log_b(MN) = \log_b M + \log_b N

Quotient Rule 

logb(MN)=logbMlogbN\log_b\bigl(\tfrac{M}{N}\bigr) = \log_b M – \log_b N

Power Rule 

logb(Mk)=klogbM\log_b(M^k) = k\,\log_b M

Change of Base 

logbN=logkNlogkb\log_b N = \tfrac{\log_k N}{\log_k b}

Inverse Relationship 

blogbN=N,logb(bx)=xb^{\log_b N} = N,\quad \log_b(b^x) = x


1.4 Applications of Logarithms in Pharmacy

  1. pH Calculation:

     

    pH=log10[H+]. \text{pH} = -\log_{10}[{\rm H}^+].

    • Example: if [H⁺] = 1.0 × 10⁻⁷ M, pH = –(–7.00) = 7.00.

  2. First‑Order Kinetics:

     

    ln ⁣(CtC0)=kt, \ln\!\bigl(\tfrac{C_t}{C_0}\bigr) = -k\,t,

    solved for k or t using natural logs.

  3. Dilution Series: plotting log concentration vs. response for calibration curves in spectrophotometry (linear relationship).


1.5 Worked Examples

  1. Factor & Simplify:
    Simplify

    4x2y2xy+6x2y3xy4x²y – 2xy + 6x²y – 3xy.

    • Combine like terms:

      (4+6)x2y+(23)xy=10x2y5xy=5xy(2x1)(4+6)x²y + (–2 –3)xy = 10x²y –5xy = 5xy(2x –1).

  2. Solve for Volume:
    Given C₁V₁ = C₂V₂: 10 M stock, need 250 mL of 0.2 M.

     

    V1=0.2×25010=5mL. V_1 = \frac{0.2\times250}{10} = 5\,\text{mL}.

  3. pH Determination:
    If an acid solution has [H⁺] = 3.16 × 10⁻⁴ M, find pH.

     

    pH=log(3.16×104)3.50. \text{pH} = -\log(3.16\times10^{-4}) \approx 3.50.

  4. First‑Order Decay:
    A drug concentration decreases from 100 mg/L to 25 mg/L in 4 h. Find k.

     

    ln ⁣25100=k×4    1.386=4k    k=0.3465h1. \ln\!\frac{25}{100} = -k\times4 \;\Longrightarrow\; -1.386 = -4k \;\Longrightarrow\; k=0.3465\,\text{h}^{-1}.


1.6 Key Points for Exams

  • Combine like terms, expand, and factor basic polynomials.

  • Apply C₁V₁=C₂V₂ algebraically for dilution calculations.

  • Know log rules: product, quotient, and power.

  • Calculate pH from hydrogen ion concentration using log 10.

  • Solve first‑order kinetics equations using natural logarithms.

 

Unit 2: Differentiation & Integration Basics

This unit introduces the fundamentals of differential and integral calculus with applications in pharmaceutical rate processes, formulation kinetics, and dosage profile analysis.


2.1 Overview of Calculus in Pharmacy

  • Differentiation: measures how a quantity changes—critical for reaction rates, dissolution rates, and pharmacokinetic rate constants.

  • Integration: computes the accumulation of a quantity—used to determine total drug released over time, area under the concentration–time curve (AUC), and cumulative dose.


2.2 Differentiation

2.2.1 Definition

  • If

    y=f(x)y = f(x), the derivative

    dydx\dfrac{dy}{dx} or

    f(x)f'(x) is the instantaneous rate of change of

    yy with respect to

    xx:

     

    f(x)=limΔx0f(x+Δx)f(x)Δx. f'(x) = \lim_{\Delta x \to 0}\frac{f(x + \Delta x) – f(x)}{\Delta x}.

2.2.2 Basic Rules

RuleFormulaExample
Constant Rule 

ddx[C]=0\dfrac{d}{dx}[C] = 0

 

ddx[5]=0\dfrac{d}{dx}[5] = 0

Power Rule 

ddx[xn]=nxn1\dfrac{d}{dx}[x^n] = n\,x^{n-1}

 

ddx[x3]=3x2\dfrac{d}{dx}[x^3] = 3x^2

Constant Multiple 

ddx[af(x)]=af(x)\dfrac{d}{dx}[a\,f(x)] = a\,f'(x)

 

ddx[4x2]=42x=8x\dfrac{d}{dx}[4x^2] = 4·2x = 8x

Sum/Difference 

ddx[f+g]=f+g\dfrac{d}{dx}[f + g] = f’ + g’

 

ddx[x2+x]=2x+1\dfrac{d}{dx}[x^2 + x] = 2x + 1

Product Rule 

ddx[fg]=fg+fg\dfrac{d}{dx}[f\,g] = f’\,g + f\,g’

 

ddx[xex]=1ex+xex=ex(1+x)\dfrac{d}{dx}[x·e^x] = 1·e^x + x·e^x = e^x(1 + x)

Quotient Rule 

ddx[fg]=fgfgg2\dfrac{d}{dx}\Bigl[\tfrac{f}{g}\Bigr] = \tfrac{f’\,g – f\,g’}{g^2}

 

ddx[xt]\dfrac{d}{dx}\bigl[\tfrac{x}{t}\bigr]

Chain Rule 

ddx[f(g(x))]=f(g(x))g(x)\dfrac{d}{dx}[f(g(x))] = f'(g(x))·g'(x)

 

ddx[e3x]=e3x3\dfrac{d}{dx}[e^{3x}] = e^{3x}·3

2.2.3 Pharmaceutical Applications

  • Dissolution Rate: if

    C(t)C(t) is drug concentration at time

    tt,

    dCdt\dfrac{dC}{dt} gives the instantaneous dissolution rate.

  • Pharmacokinetics: for first‑order elimination,

    C(t)=C0ektC(t) = C_0 e^{-k t}, differentiation yields

    dCdt=kC0ekt\dfrac{dC}{dt} = -k C_0 e^{-k t}.

  • Reaction Kinetics: rate laws expressed as

    d[A]dt=k[A]n\dfrac{d[A]}{dt} = -k [A]^n.


2.3 Integration

2.3.1 Definition

  • The integral

    f(x)dx\int f(x)\,dx represents the accumulation (area under the curve) of

    f(x)f(x) with respect to

    xx.

  • Indefinite Integral:

     

    f(x)dx=F(x)+C, \int f(x)\,dx = F(x) + C,

    where

    F(x)=f(x)F'(x) = f(x) and

    CC is the constant of integration.

  • Definite Integral:

     

    abf(x)dx=F(b)F(a), \int_{a}^{b} f(x)\,dx = F(b) – F(a),

    the net accumulation from

    x=ax=a to

    x=bx=b.

2.3.2 Basic Rules

RuleFormulaExample
Power Rule 

xndx=xn+1n+1+C\int x^n\,dx = \tfrac{x^{n+1}}{n+1} + C

 

x2dx=x33+C\int x^2\,dx = \tfrac{x^3}{3} + C

Constant Multiple 

af(x)dx=af(x)dx\int a\,f(x)\,dx = a \int f(x)\,dx

 

5xdx=5x22+C\int 5x\,dx = 5·\tfrac{x^2}{2} + C

Sum/Difference 

[f+g]dx=fdx+gdx\int [f + g]\,dx = \int f\,dx + \int g\,dx

 

(x+1)dx=x22+x+C\int (x + 1)\,dx = \tfrac{x^2}{2} + x + C

Definite Integral 

abf(x)dx=F(b)F(a)\int_{a}^{b} f(x)\,dx = F(b) – F(a)

 

012xdx=[x2]01=1\int_{0}^{1} 2x\,dx = [x^2]_0^1 = 1

2.3.3 Pharmaceutical Applications

  • Area Under Curve (AUC):

    AUC=0C(t)dt\mathrm{AUC} = \int_{0}^{\infty} C(t)\,dt quantifies total drug exposure.

  • Cumulative Release: if release rate

    r(t)r(t), cumulative amount released

    Q(t)=0tr(τ)dτQ(t) = \int_{0}^{t} r(\tau)\,d\tau.

  • Mass Balance: integrate concentration profiles to calculate total mass in a compartment over time.


2.4 Worked Examples

  1. Differentiate:

    f(x)=5x32x+7f(x) = 5x^3 – 2x + 7.

     

    f(x)=15x22. f'(x) = 15x^2 – 2.

  2. Integrate:

    (4t23)dt\int (4t^2 – 3)\,dt.

     

    4t2dt=4t33,3dt=3t;so 4t333t+C. \int 4t^2\,dt = \tfrac{4t^3}{3},\quad \int -3\,dt = -3t;\quad \text{so } \tfrac{4t^3}{3} – 3t + C.

  3. Compute AUC for

    C(t)=C0ektC(t) = C_0 e^{-k t} from

    t=0t=0 to

    \infty.

     

    AUC=0C0ektdt=C0k. \mathrm{AUC} = \int_{0}^{\infty} C_0 e^{-k t}\,dt = \frac{C_0}{k}.


2.5 Key Points for Exams

  • Apply power, sum, and chain rules to differentiate typical functions.

  • Recognize that the derivative represents rate of change, and integral gives accumulated total.

  • Use definite integrals to calculate AUC and cumulative release in pharmacokinetics.

  • Memorize basic differentiation and integration formulas and practice simple examples.

Unit 3: Elementary Statistics (Mean, Median, Mode)

This unit introduces basic statistical measures used in pharmaceutical analysis and quality control to summarize and describe data sets: the arithmetic mean, median, and mode. You’ll learn their definitions, calculation methods, interpretation, and practical examples relevant to pharmacy.


3.1 Importance of Descriptive Statistics in Pharmacy

  • Quality Control: assess uniformity of tablet weights, potency assay results, content uniformity.

  • Experimental Analysis: summarize replicate measurements (e.g., pH readings, dissolution times).

  • Data Interpretation: provide quick insights into central tendency and variability before inferential analysis.


3.2 The Arithmetic Mean (Average)

3.2.1 Definition

The arithmetic mean is the sum of all observations divided by the number of observations. It represents the “center of gravity” of the data.

 

xˉ=1ni=1nxi\bar{x} = \frac{1}{n}\sum_{i=1}^n x_i

  • xix_i: each individual value

  • nn: total number of values

3.2.2 Properties

  • Sensitive to every data point, including outliers.

  • Useful for normally distributed data.

  • The sum of deviations

    (xixˉ)(x_i – \bar{x}) equals zero.

3.2.3 Worked Example 1: Tablet Weight

Five tablets of a new formulation are weighed (mg): 198.2, 201.5, 199.8, 200.1, 199.4. Calculate the mean weight.

 

xˉ=198.2+201.5+199.8+200.1+199.45=998.05=199.6  mg\bar{x} = \frac{198.2 + 201.5 + 199.8 + 200.1 + 199.4}{5} = \frac{998.0}{5} = 199.6\;\text{mg}

Thus, the average tablet weight is 199.6 mg.

3.2.4 Worked Example 2: Assay Results

Assay of active ingredient in five samples yields (% of label claim): 98.5, 99.0, 98.8, 99.2, 98.9. Mean assay:

 

xˉ=98.5+99.0+98.8+99.2+98.95=494.45=98.88  %\bar{x} = \frac{98.5 + 99.0 + 98.8 + 99.2 + 98.9}{5} = \frac{494.4}{5} = 98.88\;\%

Average potency = 98.88 % of label claim.


3.3 The Median

3.3.1 Definition

The median is the middle value of an ordered data set. It divides the data into two equal halves.

  • For odd

    nn: median is the

    n+12\tfrac{n+1}{2}th value.

  • For even

    nn: median is the average of the

    n2\tfrac{n}{2}th and

    n2+1\tfrac{n}{2} + 1th values.

3.3.2 Properties

  • Resistant to outliers and skewed data.

  • Better measure of central tendency when data are not symmetrically distributed.

3.3.3 Worked Example 1: Dissolution Times

Eight tablets’ dissolution times (minutes) sorted: 12, 13, 14, 15, 16, 17, 18, 19.

n=8n=8, even.

  • n2=4\tfrac{n}{2} = 4 → 4th value = 15

  • 5th value = 16

 

Median=15+162=15.5  minutes\text{Median} = \frac{15 + 16}{2} = 15.5\;\text{minutes}

3.3.4 Worked Example 2: Skewed Content Uniformity

Content uniformity results (% of label) sorted for seven units: 92, 95, 96, 97, 98, 99, 105.

  • n=7n=7, odd → median is 4th value = 97 %.

  • Note the outlier (105 %) does not affect median.


3.4 The Mode

3.4.1 Definition

The mode is the value(s) that occur most frequently in a data set. A set may be:

  • Unimodal: one mode

  • Bimodal: two modes

  • Multimodal: more than two modes

  • No mode: all values occur with equal frequency

3.4.2 Properties

  • Applicable to nominal, ordinal, and numerical data.

  • Indicates the most typical or frequent observation.

3.4.3 Worked Example 1: Particle Size Distribution

Particle size measurements (µm): 50, 55, 55, 60, 60, 60, 65, 70.

  • Frequency: 60 µm appears 3 times → mode = 60 µm.

3.4.4 Worked Example 2: Excipients in Market Survey

A survey of 12 pharmacies on preferred diluent: Lactose (5), MCC (4), DCP (3). Mode = Lactose (most frequent choice).


3.5 Comparing Mean, Median, and Mode

CharacteristicMeanMedianMode
Sensitivity to OutliersHighLowNone
Data TypeInterval/ratioInterval/ratioAny (including nominal)
Calculation ComplexityModerate (sum/division)Simple (ordering)Simple (frequency count)
Best UseSymmetric distributionsSkewed distributionsCategorical data

3.6 Pharmaceutical Applications

  • Stability Data: use median to summarize degradation times when outliers (accelerated failures) occur.

  • Quality Control Charts: track mean and mode of process parameters to detect shifts.

  • Formulation Surveys: mode identifies most commonly used excipient or packaging type.


3.7 Key Points for Exams

  1. Mean: sum of values ÷ number of values; affected by every observation.

  2. Median: middle value in ordered list; robust against extremes.

  3. Mode: most frequent value; the only measure applicable to nominal data.

  4. Selection: choose median or mode for skewed or categorical data; mean for normally distributed measurement data.

  5. Example Calculations: practice with small data sets in contexts like tablet weights, assay results, and survey frequencies.

Unit 4: Pharmaceutical Calculations Review

This unit consolidates key calculation techniques used throughout pharmacy practice—including strength expressions, dilution, allegation, dose calculations, and rate/time computations—with detailed examples to reinforce proficiency.


4.1 Expression of Strength

4.1.1 Percent Strengths

  • % w/v: grams of solute per 100 mL of solution

     

    %w/v=mass of solute (g)volume of solution (mL)×100 \%\,w/v = \frac{\text{mass of solute (g)}}{\text{volume of solution (mL)}} \times 100

  • % w/w: grams of solute per 100 g of preparation

     

    %w/w=mass of solute (g)mass of preparation (g)×100 \%\,w/w = \frac{\text{mass of solute (g)}}{\text{mass of preparation (g)}} \times 100

Example 4.1: Prepare 500 mL of 2 % w/v sodium chloride.

  • Required NaCl =

    2 g/100 mL×500 mL/100=10 g2 \text{g}/100 \text{mL} × 500 \text{mL}/100 = 10 \text{g}.

4.1.2 Ratio Strength

  • Represents one part of drug per n parts of total

     

    Ratio=1:n%w/v=1n×100 \text{Ratio} = 1 : n \quad\Longrightarrow\quad \%\,w/v = \frac{1}{n} × 100

Example 4.2: A 1 : 200 solution of dextrose.

  • % w/v =

    1/200×100=0.5%1/200 × 100 = 0.5\%; thus, 0.5 g per 100 mL.


4.2 Dilution Calculations

4.2.1 Basic Dilution Formula

 

C1V1=C2V2C_1 V_1 = C_2 V_2

  • C1,V1C_1, V_1: concentration and volume of stock

  • C2,V2C_2, V_2: desired concentration and final volume

Example 4.3: From a 5 M stock, prepare 250 mL of 0.1 M solution.

 

V1=C2V2C1=0.1×2505=5 mL.V_1 = \frac{C_2 V_2}{C_1} = \frac{0.1 × 250}{5} = 5 \text{mL}.

4.2.2 Serial Dilutions

  • Stepwise dilutions to reach low concentrations.

  • Example 4.4: To achieve 1:1 000 000 from a 1:1 000 stock, perform three successive 1:100 dilutions.


4.3 Alligation

4.3.1 Alligation Medial & Alternate

  • Medial: find mean strength when ingredients are combined in known weights.

  • Alternate: determine proportions of two strengths to obtain a target strength.

Example 4.5: Mix 20 % and 5 % solutions to get 12 % final, total 100 mL.

  • Difference: |20 – 12| = 8; |12 – 5| = 7 → ratio 8 : 7.

  • Volume of 20 % =

    815×100=53.3 mL\tfrac{8}{15} × 100 = 53.3 \text{mL}, 5 % = 46.7 mL.


4.4 Dose Calculations

4.4.1 Weight‑Based Dosing

 

Patient dose=Dose per kg×Weight (kg)\text{Patient dose} = \text{Dose per kg} × \text{Weight (kg)}

Example 4.6: 5 mg/kg amoxicillin for a 20 kg child.

  • Dose = 5 mg/kg × 20 kg = 100 mg.

4.4.2 Body Surface Area (BSA) Dosing

  • Mosteller formula:

     

    BSA=Wt (kg)×Ht (cm)3600\text{BSA} = \sqrt{\frac{\text{Wt (kg)} × \text{Ht (cm)}}{3600}}

  • Example 4.7: Patient 70 kg, 170 cm:

    BSA70×17036001.8m2\text{BSA} ≈ \sqrt{\tfrac{70×170}{3600}} ≈ 1.8 m^2.

  • If drug 50 mg/m²: 50 mg/m² × 1.8 m² = 90 mg.


4.5 Flow Rate & Infusion Time

4.5.1 IV Infusion Rate

 

Rate (mL/h)=Total volume (mL)Infusion time (h)\text{Rate (mL/h)} = \frac{\text{Total volume (mL)}}{\text{Infusion time (h)}}

Example 4.8: 500 mL D5W over 4 h.

  • Rate = 500 mL ÷ 4 h = 125 mL/h.

4.5.2 Drops per Minute

  • Formula:

     

    gtt/min=Volume (mL)×Drop factor (gtt/mL)Time (min)\text{gtt/min} = \frac{\text{Volume (mL)} × \text{Drop factor (gtt/mL)}}{\text{Time (min)}}

Example 4.9: 200 mL infusion, 20 gtt/mL set, over 2 h (120 min).

  • gtt/min =

    200×20÷12033gtt/min200 × 20 ÷ 120 ≈ 33 gtt/min.


4.6 Percentage Error & Yield

4.6.1 Percentage Error

 

%Error=MeasuredTrueTrue×100\%\,\text{Error} = \frac{\lvert \text{Measured} – \text{True}\rvert}{\text{True}} × 100

Example 4.10: Tablet assay found 98 mg vs. label 100 mg.

  • % Error =

    2100×100=2%\tfrac{2}{100}×100 = 2\%.

4.6.2 Percentage Yield

 

%Yield=Actual mass obtainedTheoretical mass×100\%\,\text{Yield} = \frac{\text{Actual mass obtained}}{\text{Theoretical mass}} × 100

Example 4.11: Theoretical 50 g granules, actual yield 45 g.

  • % Yield =

    45/50×100=90%45/50×100 = 90\%.


4.7 Key Points for Exams

  • Express concentrations as % w/v, % w/w, and ratio strengths.

  • Apply C₁V₁ = C₂V₂ for dilutions and alligation for mixing.

  • Calculate patient doses using weight and BSA formulas.

  • Determine infusion rates (mL/h, gtt/min) accurately.

  • Compute percentage error and yield for quality assessments.

🧠 Tip for Students

Start with Human Anatomy & Physiology II to build on your Semester 1 foundation—understanding the body’s systems is key for all subsequent pharma subjects.

🔔 Stay updated! New unit‑wise content and practice materials added weekly.

📥 Bookmark this page for quick access to all your Semester 2 resources.

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