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Preparation and Evaluation of Charge Reversal Solid Lipid Nanoparticles
40/40 checkable references clean · checked 2026-07-23
Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.
13 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.
The 40 checked references that resolve
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Solid lipid nanoparticles (SLN) for controlled drug delivery â a review of the state of the art
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Solid lipid nanoparticles as a drug delivery system for peptides and proteins☆
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Lipid-based nanosuspensions for oral delivery of peptides, a critical review
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Design and evaluation of solid lipid nanoparticles modified with peptide ligand for oral delivery of protein drugs
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Surface modification of solid lipid nanoparticles for oral delivery of curcumin: Improvement of bioavailability through enhanced cellular uptake, and lymphatic uptake
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Effect of particle size and surface charge of nanoparticles in penetration through intestinal mucus barrier
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Zeta potential changing nanoemulsions based on a simple zwitterion
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Biomimetic Viruslike and Charge Reversible Nanoparticles to Sequentially Overcome Mucus and Epithelial Barriers for Oral Insulin Delivery
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Phosphorylated PEG-emulsifier: Powerful tool for development of zeta potential changing self-emulsifying drug delivery systems (SEDDS)
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Polyethylene imine-6-phosphogluconic acid nanoparticles – a novel zeta potential changing system
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ζ Potential Changing Nanoparticles As Cystic Fibrosis Transmembrane Conductance Regulator Gene Delivery System: an<i>In Vitro</i>Evaluation
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Zeta-potential-changing Nanoparticles Conjugated With cell-penetrating Peptides for Enhanced Transfection Efficiency
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Development of phosphorylated nanoparticles as zeta potential inverting systems
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Zeta potential changing nanoemulsions based on phosphate moiety cleavage of a PEGylated surfactant
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Charge reversal self-emulsifying drug delivery systems: A comparative study among various phosphorylated surfactants
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Zeta potential changing nanoemulsions: Impact of PEG-corona on phosphate cleavage
resolves10.1016/j.colsurfa.2013.12.023
Solid lipid nanoparticles (SLN) stabilized with polyhydroxy surfactants: Preparation, characterization and physical stability investigation
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Size shifting of solid lipid nanoparticle system triggered by alkaline phosphatase for site specific mucosal drug delivery
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Improved Method for Solid Lipid Nanoparticle Preparation Based on Hot Microemulsions: Preparation, Characterization, Cytotoxicity, and Hemocompatibility Evaluation
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IN VITRO STUDY TO EXPLAIN THE DECREASE IN ALKALINE PHOSPHATASE (ALP) ACTIVITY IN HEMOLYSED BLOOD SAMPLES FROM THE CLINICAL POINT OF VIEW.
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Distribution and Properties of Rat Intestinal Alkaline Phosphatase Isoenzymes.
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Phosphate Binding in the Active Site of Alkaline Phosphatase and the Interactions of 2-Nitrosoacetophenone with Alkaline Phosphatase-Induced Small Structural Changes
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Functional Interrelationships in the Alkaline Phosphatase Superfamily: Phosphodiesterase Activity of <i>Escherichia coli</i> Alkaline Phosphatase
resolves10.1039/D0RA03491F
A brief review on solid lipid nanoparticles: part and parcel of contemporary drug delivery systems
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Superparamagnetic nanoparticles stabilized by polymerized PEGylated coatings
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Liposome−Cell Interactions in Vitro: Effect of Liposome Surface Charge on the Binding and Endocytosis of Conventional and Sterically Stabilized Liposomes
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Surface Charge of Nanoparticles Determines Their Endocytic and Transcytotic Pathway in Polarized MDCK Cells
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Self-emulsifying peptide drug delivery systems: How to make them highly mucus permeating
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Probing the interaction of nanoparticles with mucin for drug delivery applications using dynamic light scattering
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Mucus permeating carriers: formulation and characterization of highly densely charged nanoparticles
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Development and in vitro evaluation of zeta potential changing self-emulsifying drug delivery systems for enhanced mucus permeation
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Precision cut intestinal slices are an appropriate ex vivo model to study NSAID-induced intestinal toxicity in rats
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Current State-of-Art and New Trends on Lipid Nanoparticles (SLN and NLC) for Oral Drug Delivery
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Solid lipid nanoparticles for enhanced oral absorption: A review
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Highly mucus permeating and zeta potential changing self-emulsifying drug delivery systems: A potent gene delivery model for causal treatment of cystic fibrosis
The 13 references without a DOI — listed, not checked
no DOI — not checkedref6
no DOI — not checkedCellular uptake and retention of nanoparticles: Insights on particle properties and interaction with cellular components
no DOI — not checkedref24
no DOI — not checkedref25
no DOI — not checked<em>Ex Vivo</em> Red Blood Cell Hemolysis Assay for the Evaluation of pH-responsive Endosomolytic Agents for Cytosolic Delivery of Biomacromolecular Drugs
no DOI — not checkedMucoadhesive interactions between synthetic polyaspartamides and porcine gastric mucin on the colloid size scale
no DOI — not checkedref39
no DOI — not checkedThe role of surface charge in cellular uptake and cytotoxicity of medical nanoparticles
no DOI — not checkedThiolated cyclodextrins: Mucoadhesive and permeation enhancing excipients for ocular drug delivery
no DOI — not checkedref44
no DOI — not checkedSolid lipid nanoparticles (SLN): prediction of toxicity, metabolism, fate and physicochemical properties
no DOI — not checkedref50
no DOI — not checkedOptimisation and stability assessment of solid lipid nanoparticles using particle size and zeta potential
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