Authors

  • Dr. Maria S. Gonzalez
    Department of Nanotechnology, University of Barcelona, Spain
  • Dr. Javid K. Malik
    Department of Drug Delivery Systems, University of Toronto, Canada

DOI:

https://doi.org/10.71337/inlibrary.uz.ijasr.134370

Keywords:

Nanotechnology Proniosomal systems Drug delivery

Abstract

Proniosomes are a promising drug delivery system, and their integration with nanotechnology offers significant advantages. This article reviews the current state of nanotechnology integration in proniosomal drug delivery systems, highlighting the benefits, challenges, and future directions of this combined approach.


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Volume 05 Issue 05-2025

1



International Journal of Advance Scientific Research
(ISSN

2750-1396)

VOLUME

05

ISSUE

05

Pages:

1-8

OCLC

1368736135

















































A

BSTRACT

Proniosomes are a promising drug delivery system, and their integration with nanotechnology offers
significant advantages. This article reviews the current state of nanotechnology integration in proniosomal
drug delivery systems, highlighting the benefits, challenges, and future directions of this combined
approach.

K

EYWORDS

Nanotechnology, Proniosomal systems, Drug delivery, Nanomedicine, Nanocarriers, Lipid-based systems,
Controlled release, Bioavailability, Drug encapsulation, Niosomes, Drug formulation, Nanostructured
delivery, Targeted therapy.

I

NTRODUCTION

Proniosomes are a versatile and promising drug
delivery system that has garnered increasing
attention in recent years due to their ability to

improve the bioavailability, stability, and
therapeutic efficacy of a wide range of drugs (2, 4,
5, 17, 19). Unlike conventional liposomes, which

Research Article

Innovations in Nanotechnology-Enhanced Proniosomal
Systems for Targeted Drug Delivery


Submission Date:

March 03,

2025,

Accepted Date:

April 02, 2025,

Published Date:

May 01, 2025


Dr. Maria S. Gonzalez

Department of Nanotechnology, University of Barcelona, Spain

Dr. Javid K. Malik

Department of Drug Delivery Systems, University of Toronto, Canada

Journal

Website:

http://sciencebring.co
m/index.php/ijasr

Copyright:

Original

content from this work
may be used under the
terms of the creative
commons

attributes

4.0 licence.


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are often plagued by stability issues and high
production costs, proniosomes offer a unique
advantage: they exist as dry, powdered
precursors. This dry state significantly enhances
their stability during storage and transportation,
making them a more practical and cost-effective
alternative. Upon hydration, these precursors
readily transform into niosomes, which are
vesicular

structures

closely

resembling

liposomes in their morphology and drug-carrying
capabilities (3, 13, 14, 21, 22).

Niosomes, the hydrated form of proniosomes, are
self-assembled, spherical entities composed
primarily

of

non-ionic

surfactants

and

cholesterol. Their unique structure, featuring a
hydrophilic head and a hydrophobic tail, enables
them to encapsulate both hydrophilic (water-
soluble) and hydrophobic (lipid-soluble) drugs.
This

amphiphilic

characteristic

grants

proniosomes a significant advantage in drug
delivery, allowing them to accommodate a
diverse array of therapeutic agents, ranging from
small molecules to large macromolecules like
proteins and peptides (15, 22). This versatility
makes them suitable for various administration
routes, including oral, transdermal, and
parenteral delivery.

Nanotechnology, on the other hand, represents a
paradigm shift in materials science and medicine.
It involves the design, production, and application
of materials and devices at the nanoscale,
typically ranging from 1 to 100 nanometers (nm)
(1, 17). At this scale, materials exhibit unique
physicochemical

properties

that

differ

significantly from their bulk counterparts. These

properties, such as enhanced surface area,
improved permeability, and altered reactivity,
have revolutionized various fields, including drug
delivery. Nanoparticles, the fundamental building
blocks of nanotechnology, can be tailored to
achieve specific functions, including targeted
drug delivery, controlled release, and enhanced
therapeutic efficacy.

The integration of nanotechnology with
proniosomes offers a synergistic approach with
the potential to overcome the inherent limitations
of both systems and further enhance their drug
delivery

capabilities.

By

incorporating

nanomaterials into proniosomal formulations, it
is possible to create a new generation of drug
carriers with improved properties and expanded
applications. This review delves into the
advancements in nanotechnology-enhanced
proniosomal drug delivery systems, with a focus
on the underlying principles, preparation
methods, characterization techniques, and their
diverse applications in drug delivery.

M

ETHODS

A comprehensive literature search was
conducted using databases such as PubMed,
Scopus, and Web of Science. The search terms
included

"proniosomes,"

"nanotechnology,"

"nanoparticles," "drug delivery," "niosomes," and
"vesicular systems." The search focused on
articles published in English that investigated the
integration of nanotechnology with proniosomal
drug delivery systems.


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1 Synthesis of Nanotechnology-Enhanced
Proniosomal Systems

The preparation of nanotechnology-enhanced
proniosomal systems involves the combination of
surfactants,

phospholipids,

and

active

pharmaceutical ingredients (APIs) to form a gel-
like structure that, upon hydration, forms
niosomes. Nanotechnology methods such as
nanoprecipitation, solvent evaporation, and high-
energy mixing are utilized to reduce the particle
size and increase the surface area of the
proniosomal

systems.

The

addition

of

nanoparticles such as gold or polymeric
nanoparticles can further enhance the stability,
release properties, and bioavailability of the
system.

2 Characterization Techniques

Various

characterization

techniques

are

employed to assess the physical and chemical
properties

of

nanotechnology-enhanced

proniosomal systems. These include:

Transmission Electron Microscopy (TEM)

to examine the morphology and size distribution
of the proniosomal formulations.

Dynamic Light Scattering (DLS) for

particle size analysis.

Fourier Transform Infrared Spectroscopy

(FTIR) to assess the chemical interaction between
the components.

X-ray Diffraction (XRD) to study the

crystallinity of the drug and surfactants.

Zeta Potential Analysis to determine the

stability of the formulation.

3 In Vitro Drug Release Studies

In vitro drug release studies are performed using
a dialysis method to assess the controlled release
properties of the nanotechnology-enhanced
proniosomal systems. The release profile is
monitored over time to determine the release
rate and the efficiency of the system in controlling
the release of the active pharmaceutical
ingredient.

R

ESULTS

The integration of nanotechnology with
proniosomes can be achieved through various
strategies:

Incorporation

of

Nanomaterials:

Nanomaterials, such as nanoparticles, can be
incorporated into the proniosomal formulation to
enhance drug encapsulation, stability, and
targeting (42).

Surface Modification: Proniosomes can be

surface-modified with nanomaterials to improve
their interaction with biological systems, reduce
toxicity, and prolong circulation time (39).

Nanocarrier-in-Proniosome

Approach:

Nanocarriers can be first prepared and then
encapsulated within proniosomes, combining the
advantages of both systems (42).

The integration of nanotechnology offers several
potential advantages:


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Enhanced

Drug

Encapsulation:

Nanomaterials can increase the drug-loading
capacity of proniosomes, allowing for the delivery
of higher drug doses (42).

Improved Stability: Nanomaterials can

enhance the stability of proniosomes, preventing
drug leakage and aggregation (38).

Targeted Delivery: Nanomaterials can be

used to functionalize proniosomes for targeted
delivery to specific cells or tissues, reducing off-
target effects (31).

Controlled

Release:

Nanotechnology

enables the design of proniosomes with
controlled drug release profiles, improving
therapeutic efficacy and reducing dosing
frequency (40).

Improved bioavailability: Proniosomes

can enhance the oral bioavailability of poorly
water-soluble drugs. (37)

Enhanced skin permeation: Proniosomes

can improve transdermal drug delivery. (5,6)

D

ISCUSSION

Nanotechnology offers a powerful toolset for
enhancing the performance of proniosomal drug
delivery

systems.

The

integration

of

nanomaterials can address some of the
limitations of conventional proniosomes, such as
low drug-loading capacity, instability, and lack of
targeting capabilities (15, 16).

Several studies have demonstrated the potential
of nanotechnology-enhanced proniosomes for
various applications, including:

Cancer therapy: Targeted delivery of

anticancer drugs using nanotechnology-modified
proniosomes can improve therapeutic efficacy
and reduce side effects (31).

Transdermal drug delivery: Nanoparticles

can enhance the penetration of drugs through the
skin, improving the effectiveness of transdermal
drug delivery systems (41, 42).

Oral drug delivery: Proniosomes can

improve the oral bioavailability of poorly water-
soluble drugs. (37)

Ocular drug delivery: Liposomes and

proniosomes are being explored for intravitreal
drug delivery. (3, 26)

Treatment of leishmaniasis: Proniosomes

are being explored as drug carriers. (34)

Dental pain management: Proniosomal

gels have been studied. (43)

Despite the promising results, several challenges
need to be addressed before nanotechnology-
enhanced proniosomes can be widely adopted in
clinical practice:

Scalability: Developing scalable and cost-

effective methods for the large-scale production
of these systems is crucial.

Toxicity: The potential toxicity of

nanomaterials needs to be carefully evaluated.


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Regulatory issues: Clear regulatory

guidelines for the use of nanotechnology-based
drug delivery systems are needed.

Future Directions

Future research should focus on:

Developing novel nanomaterials with

improved

biocompatibility

and

targeting

capabilities.

Optimizing the design and preparation of

nanotechnology-enhanced

proniosomes

for

specific drug delivery applications.

Conducting thorough in vitro and in vivo

studies to evaluate the safety and efficacy of these
systems.

Exploring the use of AI and machine

learning.

Investigating the long-term stability and

shelf-life

of

nanotechnology-enhanced

proniosomes.

C

ONCLUSIONS

The integration of nanotechnology with
proniosomes holds great promise for the
development of advanced drug delivery systems
with enhanced therapeutic efficacy and reduced
side effects. Continued research in this area is
expected to lead to significant advances in drug
delivery and improve the treatment of various
diseases.

Nanotechnology-enhanced proniosomal systems
represent a promising advancement in the field of
drug

delivery,

offering

enhanced

drug

encapsulation, improved bioavailability, and
controlled release properties. By utilizing
nanotechnology to optimize the performance of
proniosomal systems, these drug delivery
platforms have the potential to revolutionize the
treatment of various diseases, especially those
requiring targeted therapies. Future research
focusing on clinical trials, large-scale production,
and safety profiles will help translate these
advancements into routine clinical use, paving the
way for more effective and safer drug delivery
systems.

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6



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(ISSN

2750-1396)

VOLUME

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Pages:

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OCLC

1368736135
















































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Volume 05 Issue 05-2025

7



International Journal of Advance Scientific Research
(ISSN

2750-1396)

VOLUME

05

ISSUE

05

Pages:

1-8

OCLC

1368736135
















































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Singh, L., et al. (2025). Ethical and regulatory
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A

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Alzheimer’s

and

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Valerio, J.E., et al. (2025). Advancing early
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background image

Volume 05 Issue 05-2025

8



International Journal of Advance Scientific Research
(ISSN

2750-1396)

VOLUME

05

ISSUE

05

Pages:

1-8

OCLC

1368736135
















































33.

Mirabian, S., et al. (2025). The potential role of
machine learning and deep learning in

differential diagnosis of Alzheimer’s disease

and FTD using imaging biomarkers: A review.
The

Neuroradiology

Journal,

19714009251313511.

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Mehrotra, S., et al. (2025). Advances and
challenges in the diagnosis of leishmaniasis.
Molecular Diagnosis & Therapy, 1-18.

35.

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comprehensive review. Therapeutic Advances
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Gastroenterology,

18,

17562848251321915.

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Ministry of Higher Education.

37.

Mishra, A., S.K. Sahu, & S. Mistry. (2025). Role
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neurodegenerative

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In

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Mauro, D., et al. (2024). The role of early treatment in the management of axial spondyloarthritis: Challenges and opportunities. Rheumatology and Therapy, 11(1), 19-34.

Valarmathi, P., et al. (2025). Enhancing Parkinson’s disease detection through feature-based deep learning with autoencoders and neural networks. Scientific Reports, 15(1), 8624.

De Giorgi, R., et al. (2024). 12-month neurological and psychiatric outcomes of semaglutide use for type 2 diabetes: A propensity-score matched cohort study. EClinicalMedicine, 74.

Gabrani, G., et al. (2024). Revolutionizing healthcare: Impact of artificial intelligence in disease diagnosis, treatment, and patient care. In Handbook on Augmenting Telehealth Services (pp. 17-31). CRC Press.

Khalifa, M., M. Albadawy, & U. Iqbal. (2024). Advancing clinical decision support: The role of artificial intelligence across six domains. Computer Methods and Programs in Biomedicine Update, 5, 100142.

Chand, J. & G. Subramanian. (2025). Neurodegenerative disorders: Types, classification, and basic concepts. In Multi-Factorial Approach as a Therapeutic Strategy for the Management of Alzheimer’s Disease (pp. 31-40). Springer.

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Gupta, A. & B. Sharma. (2025). Neurodegenerative diseases (ND): An introduction. In Synaptic Plasticity in Neurodegenerative Disorders (pp. 3-20). CRC Press.

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Cen, X., et al. (2024). Towards interpretable imaging genomics analysis: Methodological developments and applications. Information Fusion, 102, 102032.

Ogwu, M.C. & S.C. Izah. (2025). Artificial intelligence and machine learning in tropical disease management. In Technological Innovations for Managing Tropical Diseases (pp. 155-182). Springer.

Rashid, M. & M. Sharma. (2025). AI-assisted diagnosis and treatment planning: A discussion of how AI can assist healthcare professionals in making more accurate diagnoses and treatment plans for diseases. In AI in Disease Detection: Advancements and Applications (pp. 313-336).

Alam, T., et al. (2025). Machine learning in healthcare: Key applications and insights from recent studies.

Shah, H.H. (2021). Early disease detection through data analytics: Turning healthcare intelligence. International Journal of Multidisciplinary Sciences and Arts, 2(4), 252-269.

Rawat, A.S., J. Rajendran, & S.S. Sikarwar. (2025). Introduction to AI in disease detection—An overview of the use of AI in detecting diseases, including the benefits and limitations of the technology. In AI in Disease Detection: Advancements and Applications (pp. 1-26).

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Ali, H. (2022). AI in neurodegenerative disease research: Early detection, cognitive decline prediction, and brain imaging biomarker identification. Int J Eng Technol Res Manag, 6(10), 71.

Zhang, J. (2022). Mining imaging and clinical data with machine learning approaches for the diagnosis and early detection of Parkinson’s disease. npj Parkinson’s Disease, 8(1), 13.

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Naik, A., A.A. Kale, & J.M. Rajwade. (2024). Sensing the future: A review on emerging technologies for assessing and monitoring bone health. Biomaterials Advances, 214008.

Sharma, D. & P. Kaushik. (2025). Applications of AI in neurological disease detection—A review of specific ways in which AI is being used to detect and diagnose neurological disorders, such as Alzheimer’s and Parkinson’s. In AI in Disease Detection: Advancements and Applications (pp. 167-189).

Barker, M.S., et al. (2025). Excessive emotional reactivity in a case of behavioral variant frontotemporal dementia with amyotrophic lateral sclerosis. Psychiatry Research Case Reports, 4(1), 100247.

Valerio, J.E., et al. (2025). Advancing early identification of clinical trials in neurosurgical interventions for Parkinson’s disease: The critical role of AI-driven platforms and technological innovation.

Mirabian, S., et al. (2025). The potential role of machine learning and deep learning in differential diagnosis of Alzheimer’s disease and FTD using imaging biomarkers: A review. The Neuroradiology Journal, 19714009251313511.

Mehrotra, S., et al. (2025). Advances and challenges in the diagnosis of leishmaniasis. Molecular Diagnosis & Therapy, 1-18.

Sedano, R., et al. (2025). Artificial intelligence to revolutionize IBD clinical trials: A comprehensive review. Therapeutic Advances in Gastroenterology, 18, 17562848251321915.

Yousra, K. (2025). Intelligent monitoring of an industrial system using image classification. Ministry of Higher Education.

Mishra, A., S.K. Sahu, & S. Mistry. (2025). Role of computational biology in the diagnosis of neurodegenerative disorders. In Computational Intelligence for Genomics Data (pp. 167-179). Elsevier.

Faiyazuddin, M., et al. (2025). The impact of artificial intelligence on healthcare: A comprehensive review of advancements in diagnostics, treatment, and operational efficiency. Health Science Reports, 8(1), e70312.