{"title":"Solid Lipid Nanoparticles in Imaging, Diagnostics and Theranostics: A Review of a decade of Innovations and Clinical Applications","authors":"Pooja Tiwary , Krishil Oswal , Ryan Varghese , Pardeep Gupta","doi":"10.1016/j.colsurfb.2025.115122","DOIUrl":null,"url":null,"abstract":"<div><div>The clinical demand for safer, more precise, and functionally versatile imaging tools has intensified with the increasing complexity of disease diagnosis and management. Despite major strides in imaging technologies such as MRI, CT, USG, and PET/SPECT, many modalities are grappled by issues including low specificity, high systemic toxicity of contrast agents, and limited ability to provide real-time functional data. Dreaded by these shortcomings, nanotechnology-based approaches such as liposomes, quantum dots (QDs), polymeric nanoparticles (NPs), gold NPs, lipid NPs, and metallic NPs have emerged as promising alternatives. Among these, solid lipid nanoparticles (SLNs) offer a unique combination of biocompatibility, structural versatility, and surface functionalizability, positioning them as advanced carriers for next-generation imaging as well as diagnostic applications, alike. SLNs are a promising nanoplatform for the delivery of imaging and diagnostic agents owing to their biocompatibility, diversity in payload encapsulation, tunable surface properties, and potential for targeted delivery. They can enhance sensitivity and specificity across imaging modalities such as MRI, PET/SPECT, CT, and optical imaging across multiple disease states. However, despite encouraging preclinical results, SLNs still face challenges such as stability, toxicity, reproducibility, and regulatory standardization, which deter their clinical application. Future research should focus on developing multifunctional SLNs for multimodal imaging, ensuring robust safety data, and concordance with regulatory standards. The integration of diagnosis and therapy, particularly in oncology, will be pivotal. Additionally, personalizing SLNs through ligand targeting may enhance their clinical feasibility and effectiveness.</div></div>","PeriodicalId":279,"journal":{"name":"Colloids and Surfaces B: Biointerfaces","volume":"257 ","pages":"Article 115122"},"PeriodicalIF":5.6000,"publicationDate":"2025-09-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Colloids and Surfaces B: Biointerfaces","FirstCategoryId":"1","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0927776525006290","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOPHYSICS","Score":null,"Total":0}
引用次数: 0
Abstract
The clinical demand for safer, more precise, and functionally versatile imaging tools has intensified with the increasing complexity of disease diagnosis and management. Despite major strides in imaging technologies such as MRI, CT, USG, and PET/SPECT, many modalities are grappled by issues including low specificity, high systemic toxicity of contrast agents, and limited ability to provide real-time functional data. Dreaded by these shortcomings, nanotechnology-based approaches such as liposomes, quantum dots (QDs), polymeric nanoparticles (NPs), gold NPs, lipid NPs, and metallic NPs have emerged as promising alternatives. Among these, solid lipid nanoparticles (SLNs) offer a unique combination of biocompatibility, structural versatility, and surface functionalizability, positioning them as advanced carriers for next-generation imaging as well as diagnostic applications, alike. SLNs are a promising nanoplatform for the delivery of imaging and diagnostic agents owing to their biocompatibility, diversity in payload encapsulation, tunable surface properties, and potential for targeted delivery. They can enhance sensitivity and specificity across imaging modalities such as MRI, PET/SPECT, CT, and optical imaging across multiple disease states. However, despite encouraging preclinical results, SLNs still face challenges such as stability, toxicity, reproducibility, and regulatory standardization, which deter their clinical application. Future research should focus on developing multifunctional SLNs for multimodal imaging, ensuring robust safety data, and concordance with regulatory standards. The integration of diagnosis and therapy, particularly in oncology, will be pivotal. Additionally, personalizing SLNs through ligand targeting may enhance their clinical feasibility and effectiveness.
期刊介绍:
Colloids and Surfaces B: Biointerfaces is an international journal devoted to fundamental and applied research on colloid and interfacial phenomena in relation to systems of biological origin, having particular relevance to the medical, pharmaceutical, biotechnological, food and cosmetic fields.
Submissions that: (1) deal solely with biological phenomena and do not describe the physico-chemical or colloid-chemical background and/or mechanism of the phenomena, and (2) deal solely with colloid/interfacial phenomena and do not have appropriate biological content or relevance, are outside the scope of the journal and will not be considered for publication.
The journal publishes regular research papers, reviews, short communications and invited perspective articles, called BioInterface Perspectives. The BioInterface Perspective provide researchers the opportunity to review their own work, as well as provide insight into the work of others that inspired and influenced the author. Regular articles should have a maximum total length of 6,000 words. In addition, a (combined) maximum of 8 normal-sized figures and/or tables is allowed (so for instance 3 tables and 5 figures). For multiple-panel figures each set of two panels equates to one figure. Short communications should not exceed half of the above. It is required to give on the article cover page a short statistical summary of the article listing the total number of words and tables/figures.