How does drug delivery affect basal metabolic rate?

Insight from top 10 papers

Drug Delivery and Basal Metabolic Rate

Basal Metabolic Rate (BMR)

BMR is the total energy expenditure of the body's tissues and organs while fasting, at rest, and under thermoneutral conditions (Verma et al., 2023). It accounts for about 25% of daily energy expenditure in sedentary subjects (Verma et al., 2023).

Factors Affecting BMR

  1. Age
  2. Gender
  3. Height
  4. Weight
  5. Body composition
  6. Physical activity
  7. Nutritional status

(Verma et al., 2023)

Drug Delivery Systems

Conventional Drug Delivery

  • Oral administration
  • Topical application
  • Intravenous injection

These methods may face challenges such as drug interactions, high metabolic rates, and toxicity (Thummamaluru, 2024).

Advanced Drug Delivery Systems

  1. Nanoparticle-based delivery
  2. Controlled release formulations
  3. Targeted drug delivery

These systems aim to improve drug efficacy and reduce side effects (Thummamaluru, 2024).

Impact of Drug Delivery on BMR

Direct Effects

  1. Metabolic rate alteration: Some drugs can directly affect the metabolic rate of cells and tissues.
  2. Hormonal changes: Drugs may influence hormone levels, which in turn affect BMR.
  3. Thermic effect: The process of drug metabolism itself may contribute to energy expenditure.

Indirect Effects

  1. Changes in body composition: Drugs may alter fat-free mass or fat mass, affecting BMR (Verma et al., 2023).
  2. Physical activity levels: Some medications may influence energy levels and physical activity, indirectly affecting BMR.
  3. Nutritional status: Drugs can impact appetite and nutrient absorption, potentially altering BMR.

Nanoparticle-based Drug Delivery and BMR

Nanoparticle-based drug delivery systems may have unique effects on BMR:

  1. Targeted delivery: By selectively targeting specific tissues or cells, nanoparticles may minimize systemic metabolic effects (Tan et al., 2021).
  2. Controlled release: Sustained drug release may lead to more stable metabolic effects over time.
  3. Enhanced cellular uptake: Improved drug absorption may result in more efficient metabolic responses with lower doses.

Polyamine Transport and BMR

Polyamine transport systems, which are upregulated in some cancer cells, may influence BMR:

  1. Increased polyamine uptake can stimulate cell growth and metabolism (Corral & Wallace, 2020).
  2. Targeting polyamine transporters for drug delivery may selectively affect the BMR of cancer cells.
  3. Modulation of polyamine transport could be a strategy to influence cellular metabolism and BMR.

Implications for Drug Development and Therapy

Personalized Medicine

Understanding the relationship between drug delivery and BMR can lead to more personalized treatment approaches:

  1. Tailoring drug dosages based on individual BMR
  2. Selecting delivery methods that minimize unwanted metabolic effects
  3. Considering BMR changes in drug efficacy and side effect profiles

Metabolic Targeting in Cancer Therapy

Exploiting differences in metabolic rates between cancer and normal cells:

  1. Using metabolic glycoengineering for tumor-targeted drug delivery (Tan et al., 2021)
  2. Developing drugs that selectively alter cancer cell metabolism
  3. Combining metabolic modulators with traditional chemotherapy for enhanced efficacy

Future Research Directions

  1. Investigating the long-term effects of various drug delivery systems on BMR
  2. Developing predictive models for drug-induced BMR changes
  3. Exploring the potential of BMR modulation as a therapeutic strategy
  4. Studying the interaction between drug delivery, BMR, and other physiological processes
Source Papers (10)
Stimuli-Responsive Boron-Based Materials in Drug Delivery
Role of Nano Particle Drug Delivery System in Antifungal Therapy
Vascularized tumor models for the evaluation of drug delivery systems: a paradigm shift
An evaluation of basal metabolic rate among healthy individuals — a cross-sectional study
Increased PIP3 activity blocks nanoparticle mRNA delivery
Exosomes as natural nanocarrier-based drug delivery system: recent insights and future perspectives
Upregulation of Polyamine Transport in Human Colorectal Cancer Cells
Understanding selectivity of metabolic labelling and click-targeting in multicellular environments as a route to tissue selective drug delivery.
Aromatized liposomes for sustained drug delivery
Poly Ethylene Glycol (PEG)‐Based Hydrogels for Drug Delivery in Cancer Therapy: A Comprehensive Review