Evidence map›Paper›PMID 42781594›Full record

ReviewInternational journal of nanomedicine2026

Bioinspired and Biomimetic Nanocarriers: Advances in Exosomes and Cell-Membrane-Coated Systems for Therapeutic Applications.

Mohamed El-Tanani, Syed Arman Rabbani, Adil Farooq Wali, Yahia El-Tanani, Zainab Zakaraya, Rakesh Kumar, Shrestha Sharma

Abstract readReview
In one paragraph

Review in International journal of nanomedicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Mohamed El-TananiRAK College of Pharmacy, Ras Al Khaimah Medical and Health Sciences University, Ras Al Khaimah, United Arab Emirates.ORCID 0000-0002-4735-5445
Syed Arman RabbaniRAK College of Pharmacy, Ras Al Khaimah Medical and Health Sciences University, Ras Al Khaimah, United Arab Emirates.ORCID 0000-0002-8454-8158
Adil Farooq WaliRAK College of Pharmacy, Ras Al Khaimah Medical and Health Sciences University, Ras Al Khaimah, United Arab Emirates.ORCID 0000-0003-1555-2820
Yahia El-TananiRoyal Cornwall Hospital Trust, NHS, Truro, TR1 3LJ, UK.
Zainab ZakarayaDepartment of Biopharmaceutics & Clinical Pharmacy, Faculty of Pharmacy, Al Ahliyya Amman University, Amman, Jordan.
Rakesh KumarAmity Institute of Pharmacy, Amity University, Panchgaon, Gurgaon, 122412, India.
Shrestha SharmaAmity Institute of Pharmacy, Amity University, Panchgaon, Gurgaon, 122412, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The translation of nanomedicine from bench to bedside has been thwarted by the limitations of conventional synthetic nanoparticles including rapid mononuclear phagocyte system (MPS) clearance, lack of target specificity, immunogenicity and poor intracellular delivery. To overcome these limitations, bioinspired and biomimetic nanocarriers are emerging as the next generation of therapeutic platforms. Bioinspired systems replicate the core biological design principles with engineered synthetic materials and biomimetic platforms use natural biological components such as cell membranes and extracellular vesicles. We herein review recent advances in bioinspired design strategies including hybrid bio-synthetic systems, and two major classes of biomimetic nanocarriers; (1) cell membrane-coated nanoparticles (CM-NPs), focusing on self-assembly approaches and their improved features over conventional fabrication methods, and (2) exosomes and extracellular vesicles (EVs), including engineered exosomes, membrane-derived vesicles, and core-shell hybrid nanocarriers. The biogenesis and isolation of exosomes and strategies for loading drugs into exosomes are discussed in depth. In particular, homotypic targeting, CD47 surface protein-mediated immune evasion, and therapeutic drug release in response to the tumor microenvironment are highlighted. Therapeutic applications of biomimetic nanocarriers in cancer, gene delivery (siRNA, mRNA, CRISPR-Cas9), neurological disorders and inflammatory diseases are covered in detail. We then discuss the challenges to translation including scalability, lot-to-lot batch reproducibility, storage stability, immunogenicity and regulatory hurdles. For the future, we discuss the role of artificial intelligence in the design of nanocarriers and personalized nanomedicine. This review outlines the advantages and disadvantages of biomimetic nanocarriers to aid in the rational design of nanomedicine for clinical translation.

Indexed as

Biomimetic MaterialsDrug CarriersExosomesNanoparticlesAnimalsBiomimeticsCell MembraneHumansNanomedicineDrug Carriersbiomimetic nanocarrierscell membrane coatingdrug deliveryexosomesextracellular vesicleshomotypic targetingimmune evasionnanomedicine

Identifiers

PMID42781594
PMCPMC13600266

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.