Evidence map›Paper›PMID 41345327›Full record

ReviewPharmaceutical research2026

Emerging Role of Nanostructured Lipid Carriers in Overcoming Cancer Treatment Challenges.

Revati T Deore

Abstract readReview
PubMed Publisher
In one paragraph

Review in Pharmaceutical research, 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

1 author.

Revati T DeoreShri Vile Parle Kelavani Mandal's Institute of Pharmacy, Tal. Dist., Dhule, Maharashtra, India. reva28patil@gmail.com.ORCID http://orcid.org/0009-0004-6717-0263

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer continues to remain a global health challenge, and conventional chemotherapy has its own limitations such as poor solubility, systemic toxicity, nonspecific biodistribution, and multidrug resistance (MDR). Nanostructured Lipid Carriers (NLCs) have proved as one of the effective drug delivery systems which can overcome all challenges of conventional technologies by enhancing therapeutic efficacy with reduced side effects. Therefore, this comprehensive review describes, in detail the structure, composition, formulation characteristics of NLCs, and manufacturing techniques. NLCs have shown significant advantages including enhanced drug solubility, controlled release characteristics, and encapsulation of hydrophilic as well as lipophilic drugs. Passive and active targeting enables NLCs to maximize the accumulation of drugs at targeted tumor sites through the enhanced permeation retention (EPR) effect. In addition, MDR targeting and long-circulating NLCs can enhance effectiveness against the resistance mechanisms of cancer cells. Cancer theranostics integrated with NLCs provide real-time diagnosis and treatment opportunities. Despite all these potential advantages, NLCs are still facing a few challenges of large-scale manufacturing, toxicity issues, and regulatory approvals. Yet, recent progress in personalized medicine and lipid-based nanotechnology reflects the potential of NLCs as a versatile and efficient delivery system for anticancer drugs. This review tries to clarify the evolving aspect of NLCs as well as the challenges faced in cancer treatment and strategies to overcome them by focusing on their ability to reshape chemotherapy and improve patient compliance.

Indexed as

Antineoplastic AgentsDrug CarriersLipidsNanostructuresNeoplasmsAnimalsDrug Delivery SystemsDrug Resistance, NeoplasmHumansAntineoplastic AgentsDrug CarriersLipidsCancerEnhanced permeability and retentionMultidrug resistanceNanostructured lipid carriersNLcs in cancer theranostics

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.