Evidence map›Paper›PMID 41165835›Full record

ReviewNaunyn-Schmiedeberg's archives of pharmacology2026

Prodrug-based drug delivery systems: strategic approaches and emerging challenges in targeted therapeutics.

Priyanka Chaturvedi, Reena Sharma, Smita Khare, Tanuja Singh, Deepa Shrivastava, Anjali Singh, Jayant Sarolia

Abstract readReview
PubMed Publisher
In one paragraph

Review in Naunyn-Schmiedeberg's archives of pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
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.

Priyanka ChaturvediDepartment of Pharmaceutics, Jai Narain College of Pharmacy, JNCT Professional University, Lambakheda, Barasia road, Bhopal, Madhya Pradesh, 462038, India.
Reena SharmaDepartment of Medicinal Chemistry, Ravishankar College of Pharmacy, New Bhanpur Bridge Rd, Bhanpur Square, Peoples Campus, Bhanpur,, Bhopal, Madhya Pradesh, 462010, India.
Smita KhareDepartment of Pharmacognosy, Ravishankar College of Pharmacy, New Bhanpur Bridge Rd, Bhanpur Square, Peoples Campus, Bhanpur, Bhopal, Madhya Pradesh, 462010, India.
Tanuja SinghDepartment of Pharmacology SunderDeep Pharmacy College, NH-24, Delhi-Hapur Road, Dasna, Gopal-Vidyanagar Campus, Ghaziabad, Uttar Pradesh, 201002, India.
Deepa ShrivastavaDepartment of Pharmacognosy, RadhaRaman College of Pharmacy, Ratibad, Madhya Pradesh, 462044, India.
Anjali SinghDepartment of Medicinal Chemistry, Ravishankar College of Pharmacy, New Bhanpur Bridge Rd, Bhanpur Square, Peoples Campus, Bhanpur,, Bhopal, Madhya Pradesh, 462010, India.
Jayant SaroliaDepartment of Pharmacology SunderDeep Pharmacy College, NH-24, Delhi-Hapur Road, Dasna, Gopal-Vidyanagar Campus, Ghaziabad, Uttar Pradesh, 201002, India. Jayant.sarolia@utu.ac.in.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prodrug-based drug delivery systems have emerged as a versatile and promising strategy for overcoming limitations associated with conventional drug formulations, such as poor solubility, low bioavailability, off-target effects, and systemic toxicity. By temporarily modifying active pharmaceutical ingredients (APIs), prodrugs can be engineered to improve therapeutic efficacy and safety profiles. This review aims to critically evaluate the current advancements, challenges, and future directions in prodrug design and delivery, with a focus on strategies that enhance pharmacokinetics, target specificity, and controlled release. Emphasis was placed on studies published over the last decade that discuss innovative prodrug approaches, delivery systems, and nanotechnology applications in drug delivery. The review categorizes prodrug strategies into two major domains: (1) chemical modification, involving covalent linkage of functional groups to alter solubility, lipophilicity, and metabolic stability, and (2) carrier-mediated delivery, employing nanocarriers such as liposomes, polymeric nanoparticles, dendrimers, and micelles to improve targeted delivery and minimize systemic exposure. While significant progress has been made, critical issues persist-such as prodrug instability, premature release, and potential toxicity. Recent innovations including rational linker design, stimuli-responsive systems, and surface-functionalized carriers have shown promise in overcoming these limitations. Prodrug-based systems have significantly advanced the field of drug delivery by enabling targeted and controlled therapeutic interventions. However, optimization of prodrug activation mechanisms and mitigation of undesired off-target effects remain ongoing challenges. Advances in prodrug design are increasingly supported by technologies such as computationally guided molecular optimization, microfluidic platforms for high-throughput screening, and the development of biomaterials with stimulus-responsive functionalities, all of which are anticipated to play a significant role in shaping the next generation of prodrug-based delivery system. Future research should focus on translational approaches that bridge laboratory success with clinical applicability.

Indexed as

Drug Delivery SystemsProdrugsAnimalsDrug CarriersHumansDrug CarriersProdrugsControlled drug releaseNanocarriersPharmacokineticsProdrugsStimuli-responsive systemsTargeted drug delivery

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.