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Biomaterial
TPO61004
Biomaterials for Drug Delivery System
Ni’matul Izza
Main reference: Ratner, 2019
Expectations?
Drug Delivery System
Definition?
Function?
Characteristics and
Properties?
Mechanism?
Challenges?
Type of drug carrier?
Delivery System
Drug Delivery System
Created by: Watanabe, N.
Goals of Drug Delivery
• Effectively treat
• Efficiently treat
Inefficiencies are considered acceptable if
there are no alternatives.
(Prime example—ocular topical therapeutics
via eye drops)
Source: google image
Drug Administration
Source: youtube channel of The Devil is in The Detail
Principles of
Pharmacokinetics
Stages of Drug Kinetics:
(L) = Liberation of drug from formulation
(A)= Absorption of drug into the blood
(D) = Distribution of drug
(M) = Metabolism of drug (liver)
(E) = Elimination of drug from body (excretion via urine)
Source: youtube channel of The Devil is in The Detail
Absorption and Release
General Rate Equation: ±
𝒅 𝑨
𝒅𝒕
= 𝒌 𝑨 𝒏
Zero Order
Rate Law: ±
𝒅 𝑨
𝒅𝒕
= 𝒌 𝑨 𝟎
= 𝒌
Integrated Profile: 𝑨 𝒕 = ±𝒌𝒕 + 𝑨 𝟎
First Order
Rate Law: ±
𝒅 𝑨
𝒅𝒕
= 𝒌 𝑨 𝟏
= 𝒌 𝑨
Integrated Profile: 𝑙𝑛 𝐴 𝑡 = ±𝒌𝒕 + 𝒍𝒏 𝑨 𝟎
𝑨 𝒕 = 𝑪𝒆±𝒌𝒕
“Bolus” Zero-Order
Pharmacokinetics refers to the movement of drug into, through, and out of the body
Challenge in Drug Delivery System
Therapeutic Index (TI) =
Drug Concentration Producing Toxic Side Effects
Minimal Drug Concentration for Therapeutic Effectiveness
Source: clinicalinfo.hiv.gov
The Issue of Patient Compliance
• Patient compliance is one of the greatest
challenges in drug delivery
• Patient compliance: the degree to which a
patient will follow a treatment plan.
Ex: poor “health literacy”, misunderstanding of side effects/
consequences, medicinal costs, forgetfulness, incompetency,
lack of trust, etc
Patient compliance should be
considered in the development of
treatment methods and drug
delivery system.
Controlled Drug
Delivery System
• The field of CDDS began in the 1960’s
• What exactly constitutes a Controlled
Drug Delivery System?
• They have predictable release
• Example: zero-order release
profiles, that have constant
release irrespective of time
Note: Not all disease models
necessitate zero-order release.
Treatment should be case-by-
case dependent fully on what
the goals of treatment are.
Source: Ratner et al., 2013
Targeted Drug
Delivery System
Overall goal: improve specificity of
treatments, particularly those with
adverse side-effect.
Ex: chemotherapy
Types of Drug Delivery System
“Nano Carrier World” !
Langmuir, 2021,
ACS App. Nano Material, 2022
(b)
(a)
(2):(3) = 1:1
10.8±3.7%
(1):(2) = 1:1
Occupied rate of (2): 50.6±15.5%
XDHPC = 0.67 with NBD
(8.8±0.2 nm)
XDHPC = 0.40 with Rhod
(22.5±0.3 nm)
XDHPC = 0.33 with NBD
(29.2±3.2 nm)
(1) (2) (3)
Liposome
/ Vesicle
SLB
Lipid Monolayer
Bicelle
Cataniosome
NLC
1
NLC
2
NLC
3
Designed
Hetero Vesicles
Nanostructured
Lipid Carrier (NLC)
Langmuir, in press
Langmuir, 2018, / CCB., in press
Langmuir,
2021, 2022
Properties and Characteristics of DDS
See you next
week!!

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NIZ_11. Biomaterials for DDS.pdf

  • 1. Biomaterial TPO61004 Biomaterials for Drug Delivery System Ni’matul Izza Main reference: Ratner, 2019
  • 3. Drug Delivery System Definition? Function? Characteristics and Properties? Mechanism? Challenges? Type of drug carrier?
  • 5. Drug Delivery System Created by: Watanabe, N.
  • 6. Goals of Drug Delivery • Effectively treat • Efficiently treat Inefficiencies are considered acceptable if there are no alternatives. (Prime example—ocular topical therapeutics via eye drops) Source: google image
  • 7. Drug Administration Source: youtube channel of The Devil is in The Detail
  • 8. Principles of Pharmacokinetics Stages of Drug Kinetics: (L) = Liberation of drug from formulation (A)= Absorption of drug into the blood (D) = Distribution of drug (M) = Metabolism of drug (liver) (E) = Elimination of drug from body (excretion via urine) Source: youtube channel of The Devil is in The Detail
  • 9. Absorption and Release General Rate Equation: ± 𝒅 𝑨 𝒅𝒕 = 𝒌 𝑨 𝒏 Zero Order Rate Law: ± 𝒅 𝑨 𝒅𝒕 = 𝒌 𝑨 𝟎 = 𝒌 Integrated Profile: 𝑨 𝒕 = ±𝒌𝒕 + 𝑨 𝟎 First Order Rate Law: ± 𝒅 𝑨 𝒅𝒕 = 𝒌 𝑨 𝟏 = 𝒌 𝑨 Integrated Profile: 𝑙𝑛 𝐴 𝑡 = ±𝒌𝒕 + 𝒍𝒏 𝑨 𝟎 𝑨 𝒕 = 𝑪𝒆±𝒌𝒕
  • 10. “Bolus” Zero-Order Pharmacokinetics refers to the movement of drug into, through, and out of the body
  • 11. Challenge in Drug Delivery System Therapeutic Index (TI) = Drug Concentration Producing Toxic Side Effects Minimal Drug Concentration for Therapeutic Effectiveness Source: clinicalinfo.hiv.gov
  • 12. The Issue of Patient Compliance • Patient compliance is one of the greatest challenges in drug delivery • Patient compliance: the degree to which a patient will follow a treatment plan. Ex: poor “health literacy”, misunderstanding of side effects/ consequences, medicinal costs, forgetfulness, incompetency, lack of trust, etc Patient compliance should be considered in the development of treatment methods and drug delivery system.
  • 13. Controlled Drug Delivery System • The field of CDDS began in the 1960’s • What exactly constitutes a Controlled Drug Delivery System? • They have predictable release • Example: zero-order release profiles, that have constant release irrespective of time Note: Not all disease models necessitate zero-order release. Treatment should be case-by- case dependent fully on what the goals of treatment are. Source: Ratner et al., 2013
  • 14. Targeted Drug Delivery System Overall goal: improve specificity of treatments, particularly those with adverse side-effect. Ex: chemotherapy
  • 15. Types of Drug Delivery System
  • 16. “Nano Carrier World” ! Langmuir, 2021, ACS App. Nano Material, 2022 (b) (a) (2):(3) = 1:1 10.8±3.7% (1):(2) = 1:1 Occupied rate of (2): 50.6±15.5% XDHPC = 0.67 with NBD (8.8±0.2 nm) XDHPC = 0.40 with Rhod (22.5±0.3 nm) XDHPC = 0.33 with NBD (29.2±3.2 nm) (1) (2) (3) Liposome / Vesicle SLB Lipid Monolayer Bicelle Cataniosome NLC 1 NLC 2 NLC 3 Designed Hetero Vesicles Nanostructured Lipid Carrier (NLC) Langmuir, in press Langmuir, 2018, / CCB., in press Langmuir, 2021, 2022
  • 17. Properties and Characteristics of DDS See you next week!!