Saji uthaman

Dr. Saji uthaman

Smart Materials and Devices (SMAD) Division, Yenepoya (Deemed to be University), Mangalore, India
orcid

Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 April 2018 in International Journal of Biological Macromolecules
Verified
Journal Article
Closed access
AMAnsuja Pulickal Mathew
Ansuja Pulickal Mathew
SUSaji uthaman
Saji uthaman
KCKi-Hyun Cho
Ki-Hyun Cho
CCChong-su Cho
Chong-su Cho
IPIn-Kyu Park
In-Kyu Park

23 August 2018 in Biomaterials Research
Verified
Journal Article
Open access
PDF file
SUSaji uthaman
Saji uthaman
KHKang Moo Huh
Kang Moo Huh
IPIn-Kyu Park
In-Kyu Park
Background: Cancer is one of the deadliest threats to human health. Abnormal physiochemical conditions and dysregulated biosynthetic intermediates in the tumor microenvironment (TME) play a significant role in modulating cancer cells to evade or defend conventional anti-cancer therapy such as surgery, chemotherapy and radiotherapy. One of the most important challenges in the development of anti-tumor therapy is the successful delivery of therapeutic and imaging agents specifically to solid tumors. Main body: The recent progresses in development of TME responsive nanoparticles offers promising strategies for combating cancer by making use of the common attributes of tumor such as acidic and hypoxic microenvironments. In this review, we discussed the prominent strategies utilized in the development of tumor microenvironment-responsive nanoparticles and mode of release of therapeutic cargo. Conclusion: Tumor microenvironment-responsive nanoparticles offers a universal approach for anti-cancer therapy.

15 June 2023 in Chemical Reviews
Verified
Journal Article
Closed access
GCGabriel Cutshaw
Gabriel Cutshaw
SUSaji uthaman
Saji uthaman
NHNora Hassan
Nora Hassan
SKSiddhant Kothadiya
Siddhant Kothadiya
XWXiaona Wen
Xiaona Wen
RBRizia Bardhan
Rizia Bardhan

3 September 2018 in Polymers
Verified
Journal Article
Open access
PDF file
VVVEENA VIJAYAN
VEENA VIJAYAN
SUSaji uthaman
Saji uthaman
IPIn-Kyu Park
In-Kyu Park
Biomimetic functionalization of nanoparticles through camouflaging with cellular membranes has emerged as a promising strategy for cancer theragnostics. Cellular membranes used for camouflaging nanoparticles are generally isolated from blood cells, immune cells, cancer cells, and stem cells. The camouflaging strategy of wrapping nanoparticles with cellular membranes allows for superior tumor targeting through self-recognition, homotypic targeting and prolonged systematic circulation, thereby aiding in effective tumor therapy. In this review, we emphasized the various types of cellular membrane-camouflaged nanoparticles, their mechanisms in targeted therapy and various biomimetic strategies for anti-cancer therapy.

23 September 2020 in Molecules
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Journal Article
Open access
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AMAyeskanta Mohanty
Ayeskanta Mohanty
SUSaji uthaman
Saji uthaman
IPIn-Kyu Park
In-Kyu Park
Cancer represents one of the most dangerous diseases, with 1.8 million deaths worldwide. Despite remarkable advances in conventional therapies, these treatments are not effective to completely eradicate cancer. Nanotechnology offers potential cancer treatment based on formulations of several nanoparticles (NPs). Liposomes and polymeric nanoparticle are the most investigated and effective drug delivery systems (DDS) for cancer treatment. Liposomes represent potential DDS due to their distinct properties, including high-drug entrapment efficacy, biocompatibility, low cost, and scalability. However, their use is restricted by susceptibility to lipid peroxidation, instability, burst release of drugs, and the limited surface modification. Similarly, polymeric nanoparticles show several chemical modifications with polymers, good stability, and controlled release, but their drawbacks for biological applications include limited drug loading, polymer toxicity, and difficulties in scaling up. Therefore, polymeric nanoparticles and liposomes are combined to form polymer-lipid hybrid nanoparticles (PLHNPs), with the positive attributes of both components such as high biocompatibility and stability, improved drug payload, controlled drug release, longer circulation time, and superior in vivo efficacy. In this review, we have focused on the prominent strategies used to develop tumor targeting PLHNPs and discuss their advantages and unique properties contributing to an ideal DDS.

1 January 2015 in BioMed Research International
Verified
Journal Article
Open access
PDF file
SUSaji uthaman
Saji uthaman
SLSangjoon Lee
Sangjoon Lee
Kondareddy CherukulaKondareddy Cherukula
Kondareddy Cherukula
CCChong-su Cho
Chong-su Cho
IPIn-Kyu Park
In-Kyu Park
Today, nanotechnology plays a vital role in biomedical applications, especially for the diagnosis and treatment of various diseases. Among the many different types of fabricated nanoparticles, magnetic metal oxide nanoparticles stand out as unique and useful tools for biomedical applications, because of their imaging characteristics and therapeutic properties such as drug and gene carriers. Polymer-coated magnetic particles are currently of particular interest to investigators in the fields of nanobiomedicine and fundamental biomaterials. Theranostic magnetic nanoparticles that are encapsulated or coated with polymers not only exhibit imaging properties in response to stimuli, but also can efficiently deliver various drugs and therapeutic genes. Even though a large number of polymer-coated magnetic nanoparticles have been fabricated over the last decade, most of these have only been used for imaging purposes. The focus of this review is on polysaccharide-coated magnetic nanoparticles used for imaging and gene delivery.