๐Ÿ“˜ Lacture -5 Factors Affecting Drug Metabolism Including Stereochemical Aspects (Medicinal Pharmaceutical Chemistry – Semester IV)

 

๐Ÿ“˜ Factors Affecting Drug Metabolism

Including Stereochemical Aspects

(Medicinal Pharmaceutical Chemistry – Semester IV)


๐ŸŒŸ Introduction

Have you ever wondered why the same drug behaves differently in different patients?
Or why one enantiomer of a drug is more active than the other?

The answer lies in drug metabolism and its influencing factors, including an important and often asked topic — stereochemical aspects of drug metabolism.

This topic is high-yield for exams and very important for understanding real clinical practice.


๐Ÿ”ฌ What is Drug Metabolism?

Drug metabolism is the biochemical modification of drugs by enzymes, mainly in the liver, to make them:

✔ More water-soluble
✔ Easier to excrete
✔ Pharmacologically less active (in most cases)

๐Ÿ“Œ Exam definition:

Drug metabolism is the enzymatic conversion of lipophilic drugs into more polar metabolites.


๐Ÿง  Factors Affecting Drug Metabolism


1️⃣ Age

๐Ÿ‘ถ Neonates & Infants:

  • Immature liver enzymes

  • Slower metabolism

  • Higher risk of toxicity

Example:
๐Ÿ‘‰ Chloramphenicol → Gray baby syndrome

๐Ÿ‘ด Elderly:

  • Reduced hepatic blood flow

  • Decreased enzyme activity

๐Ÿ“Œ Dose adjustment is required.


2️⃣ Genetic Factors (Pharmacogenetics)

Genetic variation causes differences in enzyme activity.

Types:

  • Fast metabolizers

  • Slow metabolizers

Example:
๐Ÿ‘‰ Isoniazid

  • Slow acetylators → Toxicity

  • Fast acetylators → Reduced therapeutic effect

๐Ÿ“Œ Very common viva + theory question


3️⃣ Diet & Environmental Factors

  • Smoking → Enzyme induction

  • Alcohol → Alters metabolism

  • Food components → Enzyme inhibition or induction

Example:
๐Ÿ‘‰ Grapefruit juice inhibits CYP3A4 enzymes.


4️⃣ Drug–Drug Interactions

๐Ÿ”น Enzyme Inducers:

  • Rifampicin

  • Phenobarbital

  • Phenytoin

➡ Decrease plasma drug concentration

๐Ÿ”น Enzyme Inhibitors:

  • Cimetidine

  • Ketoconazole

  • Erythromycin

➡ Increase toxicity risk


5️⃣ Liver Function

Liver is the major site of metabolism.

  • Hepatitis

  • Cirrhosis

  • Fatty liver disease

๐Ÿ“Œ Metabolism is reduced → Dose reduction needed.


6️⃣ Route of Administration

  • Oral drugs → First-pass metabolism

  • IV drugs → Bypass liver initially

Example:
๐Ÿ‘‰ Nitroglycerin is ineffective orally due to extensive first-pass metabolism.


7️⃣ Dose & Frequency

  • High dose → Enzyme saturation

  • Repeated dosing → Enzyme induction

๐Ÿ“Œ Important in chronic therapy.


๐Ÿ”„ Stereochemical Aspects of Drug Metabolism

Most important & scoring section


๐Ÿงช What is Stereochemistry in Drug Metabolism?

Many drugs exist as enantiomers (mirror-image forms).

๐Ÿ“Œ The body does not metabolize both enantiomers equally.


๐Ÿ”ฌ Enantioselective Metabolism

  • Drug-metabolizing enzymes are chiral

  • They show stereoselectivity

➡ One enantiomer may be:
✔ Metabolized faster
✔ More active
✔ More toxic


๐Ÿ“Œ Important Examples

๐Ÿ”น Propranolol

  • S-enantiomer → More pharmacologically active

  • R-enantiomer → Metabolized differently


๐Ÿ”น Warfarin

  • S-warfarin → More potent anticoagulant

  • Metabolized faster than R-enantiomer


๐Ÿ”น Thalidomide

  • One enantiomer → Therapeutic

  • Other enantiomer → Teratogenic

๐Ÿ“Œ Classic example in exams.


๐Ÿง  Why Stereochemical Aspects Matter?

✔ Explains variation in drug response
✔ Helps in safer drug design
✔ Basis of chiral switching in modern drugs
✔ Improves therapeutic efficacy


✍️ Exam-Ready Answer (Write This!)

Drug metabolism is affected by age, genetic factors, diet, drug interactions, liver function, route of administration, and dose. Additionally, stereochemical aspects play a crucial role, as drug-metabolizing enzymes are chiral and show enantioselective metabolism, leading to differences in activity, toxicity, and clearance of drug enantiomers.

Full marks guaranteed


๐Ÿงฉ MCQ Section 

Q. Which factor is responsible for enantioselective drug metabolism?
A) Dose
B) Route of administration
C) Chiral enzymes ✔
D) Liver blood flow

๐Ÿ‘‰ Answer in comments!

๐Ÿ“Œ Question for You:

Why is S-warfarin more potent than R-warfarin?
๐Ÿ‘‡ Comment your answer below.

๐Ÿ”— Internal Links 

  • Drug Metabolism: Phase I

  • Drug Metabolism: Phase II

  • First-Pass Metabolism

  • Pharmacogenetics (Coming Next)


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