Synthetic biology innovations in designing cellulose-based smart drug delivery systems

The integration of synthetic biology with cellulose-based materials has paved the way for groundbreaking advancements in smart drug release and delivery systems. Synthetic biology, through precise genetic engineering and the creation of programmable biological circuits, enables the development of drug carriers that can respond dynamically to specific physiological cues, such as pH changes. For example, the contrast in pH between the stomach (pH ~1.5 to 3.5) and the intestines (pH ~6 to 7.5) has been exploited in cellulose-based systems to achieve site-specific drug release. Cellulose offers an ideal platform for constructing these responsive drug delivery systems. This review explores recent innovations in genetically engineered cellulose, functionalization strategies via synthetic biology, and advanced biofabrication techniques such as 3D bioprinting and microfluidics. Applications of these systems span cancer therapeutics, antimicrobial treatments, chronic disease management, and emerging areas like personalized medicine and gene therapy. Challenges related to biocompatibility, scalability, and regulatory approval persist. Future directions involving CRISPR-Cas9-mediated cellulose modification, machine learning for optimized drug release, and sustainable production strategies highlight the transformative potential of these systems in precision medicine. This review provides comprehensive insights into the current state and future prospects of cellulose-based smart drug delivery, offering a roadmap for advancing next-generation therapeutics.

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Publication Details

Journal
BioResources
Published
2025-04-17
DOI
https://doi.org/10.15376/biores.20.2.selim
Citations
3
Primary Topic
Enzyme Catalysis and Immobilization
Type
article
Field-Weighted Citation Impact
2.42
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article

Synthetic biology innovations in designing cellulose-based smart drug delivery systems

Samy Selim, Soad K. Al Jaouni, Mohammad Harun‐Ur‐Rashid, Mohammed S. Almuhayawi
3 citations
BioResources
Enzyme Catalysis and Immobilization
2.42
article

Synthetic biology innovations in designing cellulose-based smart drug delivery systems

Samy Selim, Soad K. Al Jaouni, Mohammad Harun‐Ur‐Rashid, Mohammed S. Almuhayawi
article en
3 citations

Abstract

The integration of synthetic biology with cellulose-based materials has paved the way for groundbreaking advancements in smart drug release and delivery systems. Synthetic biology, through precise genetic engineering and the creation of programmable biological circuits, enables the development of drug carriers that can respond dynamically to specific physiological cues, such as pH changes. For example, the contrast in pH between the stomach (pH ~1.5 to 3.5) and the intestines (pH ~6 to 7.5) has been exploited in cellulose-based systems to achieve site-specific drug release. Cellulose offers an ideal platform for constructing these responsive drug delivery systems. This review explores recent innovations in genetically engineered cellulose, functionalization strategies via synthetic biology, and advanced biofabrication techniques such as 3D bioprinting and microfluidics. Applications of these systems span cancer therapeutics, antimicrobial treatments, chronic disease management, and emerging areas like personalized medicine and gene therapy. Challenges related to biocompatibility, scalability, and regulatory approval persist. Future directions involving CRISPR-Cas9-mediated cellulose modification, machine learning for optimized drug release, and sustainable production strategies highlight the transformative potential of these systems in precision medicine. This review provides comprehensive insights into the current state and future prospects of cellulose-based smart drug delivery, offering a roadmap for advancing next-generation therapeutics.

BioResourcesVol. 20(2)
King Abdulaziz University (SA), Jouf University (SA), International University of Business Agriculture and Technology (BD)
Openalex Percentile: Top 12%
Enzyme Catalysis and Immobilization
2.42
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