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A peer-reviewed article of this preprint also exists.
This version is not peer-reviewed
Submitted:
05 December 2023
Posted:
06 December 2023
You are already at the latest version
Applicant Name | % documents | Country |
---|---|---|
Noven Pharma | 4.3 | USA |
Alza Corp | 3.1 | USA |
3M Innovative Properties Co | 2.0 | USA |
Univ California | 1.0 | USA |
Acrux Dds Pty LTD | 1.0 | Australia |
Mylan Technologies INC | 0.9 | USA |
Kimberly Clark Co | 0.9 | USA |
Corium Int INC | 0.8 | USA |
Chrono Therapeutics INC | 0.8 | USA |
Koninkl Philips Electronics Nv | 0.7 | Holland |
Rank | Source | IF (2022) | Total publications (Percentage) |
Total Citations |
---|---|---|---|---|
1 | International Journal of Pharmaceutics | 6.270 | 525 (6.7 %) | 23,596 |
2 | Journal Of Controlled Release | 11.467 | 262 (3.4 %) | 19,315 |
3 | Journal Of Pharmaceutical Sciences | 3.534 | 226 (2.9 %) | 6,606 |
4 | Drug Development and Industrial Pharmacy | 3.225 | 178 (2.3 %) | 4,365 |
5 | AAPS Pharmscitech | 3.246 | 158 (2.0 %) | 4,451 |
6 | Journal Of Drug Delivery Science and Technology | 3.981 | 155 (2.0 %) | 1,837 |
7 | Pharmaceutical Research | 4.580 | 153 (2.0 %) | 7,893 |
8 | Pharmaceutics | 6.072 | 135 (1.7 %) | 1,724 |
9 | European Journal of Pharmaceutics and Biopharmaceutics | 5.589 | 126 (1.6 %) | 6,486 |
10 | Drug Delivery | 6.420 | 122 (1.6 %) | 2,462 |
Title | PY | Journal | Citations | Ref. |
---|---|---|---|---|
Biomedical applications of collagen | 2001 | International Journal of Pharmaceutics | 1,516 | [16] |
Penetration enhancers | 2012 | Advanced Drug Delivery Reviews | 1,509 | [17] |
Microneedles for transdermal drug delivery | 2004 | Advanced Drug Delivery Reviews | 1,102 | [18] |
Ethosomes - Novel vesicular carriers for enhanced delivery: Characterization and skin penetration properties | 2000 | Journal of Controlled Release | 1,044 | [19] |
Biodegradable polymer microneedles: Fabrication, mechanics, and transdermal drug delivery | 2005 | Journal of Controlled Release | 693 | [20] |
Wearable/disposable sweat-based glucose monitoring device with multistage transdermal drug delivery module | 2017 | Science Advances | 679 | [21] |
Microfabricated needles for transdermal delivery of macromolecules and nanoparticles: Fabrication methods and transport studies | 2003 | Proceedings of the National Academy of Sciences of the United States of America | 658 | [22] |
Iontophoretic drug delivery | 2004 | Advanced Drug Delivery Reviews | 641 | [23] |
Dissolving microneedles for transdermal drug delivery | 2008 | Biomaterials | 639 | [24] |
Lipid vesicles and other colloids as drug carriers on the skin | 2004 | Advanced Drug Delivery Reviews | 573 | [25] |
Author Name | Country | Affiliation | Documents count |
---|---|---|---|
Banga, A.K. | United States | University of Atlanta | 78 |
Donnelly, R.F. | Ireland | Queen’s University Belfast | 75 |
Prausnitz, M.R. | United States | Georgia Institute of Technology | 69 |
Kalia, Y.N. | Suisse | Université de Genève | 61 |
Fang, L. | China | Shenyang Pharmaceutical University | 58 |
Mitragotri, S. | United States | Georgia Institute of Technology | 50 |
Aqil, M. | Saudi Arabia | King Saud University | 49 |
Stinchcomb, A.L. | United States | University of Maryland School of Pharmacy | 46 |
Opanasopit, P. | Thailand | Silpakorn University | 38 |
Shin, S.C. | South Korea | Chonnam National University | 38 |
Funding Sponsor | Country | Documents count |
---|---|---|
National Natural Science Foundation | China | 469 |
National Institutes of Health | United States | 237 |
National Research Foundation | Korea | 117 |
National Institute of Biomedical Imaging and Bioengineering | United States | 79 |
Fundamental Research Funds for the Central Universities | China | 74 |
Japan Society for the Promotion of Science | Japan | 72 |
Conselho Nacional de Desenvolvimento Científico e Tecnológico | Brasil | 70 |
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior | Brasil | 70 |
National Science Foundation | United States | 70 |
Ministry of Education, Culture, Sports, Science and Technology | Japan | 64 |
Subject Area | Documents count |
---|---|
Pharmacology, Toxicology and Pharmaceutics | 4,778 |
Medicine | 1,790 |
Biochemistry, Genetics and Molecular Biology | 1,553 |
Chemistry | 1,337 |
Materials Science | 1,132 |
Engineering | 852 |
Chemical Engineering | 791 |
Physics | 509 |
Immunology and Microbiology | 134 |
Multidisciplinary | 124 |
Keywords | ||||||
---|---|---|---|---|---|---|
Cluster 1 | Cluster 2 | Cluster 3 | Cluster 4 | Cluster 5 | Cluster 6 | |
anti-inflammatory curcumin diclofenac sodium dissolving MNs ethosome hyaluronic acid hydrogel ibuprofen in vitro release indomethacin ketoprofen liposome meloxicam methotrexate microemulsion nanoemulsion nanoparticle |
nanostructured lipid carriers oleic acid penetration enhancer percutaneous absorption psoriasis rheumatoid arthritis skin irritation skin penetration skin permeability skin permeation solid lipid nanoparticles stability stratum corneum sustained release topical delivery transdermal absorption transdermal permeation |
bioavailability buprenorphine enhancer estradiol fentanyl human skin lidocaine microdialysis pain patch pharmacodynamics pharmacokinetic transdermal administration transdermal delivery system transdermal patch |
absorption controlled release diclofenac diffusion drug delivery systems formulation hydrogels mathematical model percutaneous permeability protein delivery skin solubility surfactants |
chitosan drug release flux hypertension in vitro in vivo nanoparticles permeation permeation enhancer release topical transdermal transdermal patches |
diabetes drug delivery electroporation insulin iontophoresis microneedles sonophoresis ultrasound |
ethosomes factorial design gel liposomes niosomes optimization proniosomes transfersomes |
Drug/prodrug/NPs Released | Methods of Preparation and Formulation Details | System Operation | Inference | Cluster | Ref. |
---|---|---|---|---|---|
Ammonium glycyrrhizinate (A.G.) | Ammonium glycyrrhizinate - ultra-deformable liposomes (A.G.-ULs) were obtained by dissolving the drug in the lipid components during the synthesis of ULs (thin-layer evaporation technique) | High dimensional stable ULs pass intact through the skin and deliver AG in specific tissues in a controlled manner | Anti-inflammatory effect | 6 | [58] |
Resveratrol/ caffeic acid containing glycoconjugates | Imbibition of PEGDA/HEMA films in water solution containing the glycoconjugates | pH-dependent release of synthetic selenium-containing glycoconjugates | Antioxidant effect, potential wound healing acceleration | 3 | [59] |
Horseradish peroxidase (HRP) enzyme | Silk MNs obtained by aqueous-based micro-molding and simultaneous loading with HRP | The degradation rate of silk fibroin and the diffusion rate of the entrained molecules can be controlled by adjusting post-processing conditions | Tunable release kinetics | 5 | [60] |
Lidocaine hydrochloride (LIDH) | UV crosslinked methacrylated chondroitin sulfate (CS-MA) and polyvinylpyrrolidone (PVP) K29/32MNs loaded with LIDH | At body temperature PVP K29/32 rapidly dissolve, with subsequent release of LIDH | Local anesthesia | 5 | [61] |
Ibuprofenamine hydrochloride (2-(Diethylamino) ethyl 2-(4-isobutylphenyl) propionate hydrochloride | Clinical trial research, in which spray Ibuprofenamine hydrochloride penetrates the skin and biological barrier into the lesion tissue after administration | Spray Ibuprofenamine hydrochloride (prodrug of ibuprofen) penetrates the skin and is quickly converted into therapeutic ibuprofen | Anti-inflammatory effect | 1 | [31] |
Ibuprofen | Hot-melt poly(ether-urethane)-silicone crosslinked pressure-sensitive adhesive (HMPSAs) drug reservoir formation | Adhesive matrix releases ibuprofen that penetrates the skin. The presence of chemical enhancers, di(ethylene) glycol monoethyl ether (DEGEE), facilitates the API penetration | Anaesthetic in case of moderate pain | 1 | [62]x |
Buprenorphine hydrochloride (Bup) | Electrospinning of poly (vinyl pyrrolidone) (PVP) and a blend of 50/50 W/W of buprenorphine-loaded poly(vinyl alcohol (PVA) and PVP polymer solutions in water, used as a drug carrier for buprenorphine (Bup): (Bup/PVP) and(Bup/PVP/PVA) | Bup-loaded crosslinked nanofibers improve carrier retention and provide a controlled release of Bup | Controlled release | 2 | [63] |
Fentanyl citrate | Sucrose based MN model are made from a water-soluble matrix, premixed with fentanyl citrate | Dissolving MNs are submerged in a rectangular compartment. The top and the bottom of the compartment represent the SC and the bloodstream, respectively. Once an MN patch is applied to the skin, the needles penetrate the dermis and begin to dissolve. | Controlled release | 2 | [64] |
Ampicillin sodium | Polyvinyl alcohol (PVA)/ chitosan (CS) composite nanofibers are fabricated by electrospinning, and then crosslinked through glulataraldehyde (GA) | Crosslinked PVA/CS composite nanofibers have a lower drug release rate and a smaller amount of drug burst release than that of PVA/CS, showing potential as TDD system | Controlled release of drugs | 4 | [65] |
5-FU anti-cancer drug | 5-fluorouracil-chitosan-carbon quantum dot-aptamer (5-FU-CS-CQD-Apt) nanoparticle is synthesized owing to W/O emulsification method | 5-FU-CS-CQD-Apt shows a pH-sensitive and sustained drug release profile | Release of the drug in a controlled manner | 4 | [66] |
Piroxicam | Nanoprecipitation technique is used for preparation of drug loaded Eudragit S100 (ES100)/NPs. | ES100 as a nanocarrier for transdermal delivery of Piroxicam | pH-sensitive permeation | 3 | [67] |
Celecoxib (CXB) | CXB niosomes by thin film hydration method | The release of CXB from different niosomal gel formulations (Span 60 or Span 40 and cholesterol) depends on the viscosity of the prepared gels | Anti-inflammatory activity of the drug from niosomal gel formulations | 1,6 | [68] |
Jurisdiction | Documents Count |
---|---|
United States | 3,002 |
China | 793 |
European Patents | 608 |
Canada | 268 |
Korea, Republic of | 222 |
Australia | 207 |
Japan | 90 |
Mexico | 84 |
Taiwan | 68 |
United Kingdom | 37 |
CPC | % |
---|---|
A61K9/0014 | 10.6 |
A61K9/7061 | 8.2 |
A61P29/00 | 6.0 |
A61M37/0015 | 5.8 |
A61K9/7084 | 5.8 |
A61P35/00 | 5.4 |
A61K47/10 | 5.3 |
A61K45/06 | 4.9 |
A61P43/00 | 4.7 |
A61P25/00 | 4.5 |
Application Number | Application Date | Title | Owners | Rif |
---|---|---|---|---|
US 10 303 851 B2 | 14/03/2014 | Physician-centric health care delivery platform | HANA PATENT TECHNOLOGY LLC | [75] |
US 8 523 791 B2 | 11/08/2009 | Multi-modal drug delivery system | CAREWEAR CORP | [76] |
US 9 375 529 B2 | 02/09/2009 | Extended use medical device | BECTON DICKINSON AND COMPANY | [77] |
US 8 372 040 B2 | 24/05/2006 | Portable drug delivery device including a detachable and replaceble administration or dosing element | CHRONO THERAPEUTICS INC | [78] |
US 8 617 071 B2 | 31/10/2006 | Analyte monitoring device and methods of use | ABBOTT DIABETES CARE INC | [69] |
US 8 252 321 B2 | 31/10/2007 | Biosynchronous transdermal drug delivery for longevity, anti-aging, fatigue management, obesity, weight loss, weight management, delivery of nutraceuticals, and the treatment of hyperglycemia, alzheimer’s disease, sleep disorders, parkinson’s disease, aids, epilepsy, attention deficit disorder, nicotine addiction, cancer, headache and pain control, asthma, angina, hypertension, depression, cold, flu and the like | CHRONO THERAPEUTICS INC | [79] |
US 7 658 728 B2 | 10/01/2006 | Microneedle array, patch, and applicator for transdermal drug delivery | YUZHAKOV VADIM V | [80] |
US 9 186 372 B2 | 21/05/2013 | Split dose administration | MODERNA THERAPEUTICS | [81] |
WO 2004/060436 A2 | 04/12/2003 | Skin attachament apparatus and method for patient infusion device | INSULET CORP | [82] |
US 7 206 632 B2 | 30/01/2004 | Patient sensory response evaluation for neuromodulation efficacy rating | MEDTRONIC INC | [83] |
Application Number | Application Date | Title | Owners | Note on TDD | Ref. |
---|---|---|---|---|---|
US 7 871 607 B2 | 23/02/2005 | Soluble glycosaminoglycanases and methods of preparing and using soluble glycosaminoglycanases | HALOZYME INC | Novel soluble neutral active Hyaluronidase Glycoproteins (sHASEGPs), methods of manufacture and administration (including TDD) that can be applied to enhance the bioavailability (and potentially improve other pharmacokinetic and / or pharmacodynamic properties) of pharmacologic and other agents that are useful for treating or diagnosing various disease conditions | [84] |
WO 2004/39826 A1 | 26/10/2002 | Anti-il-6 antibodies, compositions, methods and uses | CENTOCOR INC | Transdermal administration of anti-IL-6 antibody encapsulated in a delivery device such as a liposome or polymeric nanoparticles, microparticle, microcapsule, or microspheres (referred to collectively as microparticles unless otherwise stated) | [85] |
US 11 154 559 B2 | 28/09/2012 | Methods and compositions of bile acids | GEN HOSPITAL CORP | A carrier that protects the composition against rapid release, such as a controlled release formulation, including implants, transdermal patches, and microencapsulated delivery systems | [86] |
WO 2004/002417 A2 | 27/06/2003 | Mammalian CH1 deleted mimetibodies, compositions, methods and uses | CENTOCOR INC | CH1-deleted mimetibody or specified portion or variant in either the stable or preserved formulations or solutions described, can be administered via a variety of delivery methods including TDD | [87] |
US 7 985 424 B2 | 21/12/2005 | Dendritic polymers with enhanced amplification and interior functionality | DENDRITIC NANOTECHNOLOGIES INC | Dendritic polymers can have utility in many application (in vivo diagnostic imaging, drug delivery, drug discovery, in vitro diagnostics, coatings for medical devices, anti-biofouling coatings, TDD, chemotherapies, NIR absorbers, magnetic bioreactor, etc. | [88] |
WO 2005/032460 A2 | 03/09/2004 | Human epo mimetic hinge core mimetibodies, compositions, methods and uses | CENTOCOR INC | Mammalian EPO mimetic hinge core mimetibodies that can be used by contacting or administering by at least one mode comprising TDD | [89] |
WO 2004/037225 A2 | 24/10/2003 | Cosmetic and pharmaceutical foam | FOAMIX LTD | Alcohol-free, pharmaceutical foam carrier and its use | [90] |
US 7 591 806 B2 | 18/05/2005 | High-aspect-ratio microdevices and methods for transdermal delivery and sampling of active substances | XU BAI | High-aspect-ratio microdevices (including microneedles) and the method of making and using the same, for TDD | [91] |
WO 01/95935 A1 | 22/01/2001 | Immunostimulatory nucleic acids for inducing a th2 immune response | OTTAWA HEALTH RESEARCH INST | The compounds can be administered to the skin, e.g., topically in the form of a skin cream, by injection, or any other method of administration where access to the skin cells and/or target APCs by the compounds is obtained | [92] |
US 8 372 040 B2 | 22/01/2001 | Portable drug delivery device including a detachable and replaceable administration or dosing element | CHRONO THERAPEUTICS INC | A device for TDD and administration of differing dosages at specific times of the day automatically pursuant to a pre-programmed dosage profile | [78] |
Application Number |
Application Date |
Title | Owners | Note | Ref. |
---|---|---|---|---|---|
US 7 871 607 B2 | 23/02/2005 | Soluble glycosaminoglycanases and methods of preparing and using soluble glycosaminoglycanases | HALOZYME INC | Novel soluble neutral active Hyaluronidase Glycoproteins (sHASEGPs), methods of manufacture and administration (including TDD) that can be applied to enhance the bioavailability (and potentially improve other pharmacokinetic and / or pharmacodynamic properties) of pharmacologic and other agents that are useful for treating or diagnosing various disease conditions | [84] |
US 7 985 424 B2 | 21/12/2005 | Dendritic polymers with enhanced amplification and interior functionality | DENDRITIC NANOTECHNOLOGIES INC | Dendritic polymers can have utility in many application (in vivo diagnostic imaging, drug delivery, drug discovery, in vitro diagnostics, coatings for medical devices, anti-biofouling coatings, TDD, chemotherapies, NIR absorbers, magnetic bioreactor, etc. | [88] |
WO2012118562A1 | 02/03/2012 | Compositions and methods for treating depression, adhd and other central nervous system disorders employing novel bupropion compounds, and methods for production and use of novel bupropion compounds and formulations | RHINE PHARMACEUTICALS LLC | Compositions and methods are disclosed using a purified (R)(-) enantiomer of bupropion (including prodrug) to treat central nervous system disorders | [93] |
WO 2004/037225 A2 | 24/10/2003 | cosmetic and pharmaceutical foam | FOAMIX LTD | Alcohol-free, pharmaceutical foam carrier and its use | [90] |
US 8 523 791 B2 | 11/08/2009 | Multi-modal drug delivery system | CAREWEAR CORP | A device for the transdermal delivery of a therapeutic agent at a treatment site comprising a mechanical vibration element, a light source, and a heating and/or cooling element | [76] |
WO 01/95935 A1 | 22/01/2001 | Immunostimulatory nucleic acids for inducing a th2 immune response | OTTAWA HEALTH RESEARCH INST | The compounds can be administered to the skin, e.g., topically in the form of a skin cream, by injection, or any other method of administration where access to the skin cells and/or target APCs by the compounds is obtained | [92] |
US 10 369 204 B2 | 02/10/2009 | Molecular vaccines for infectious disease | AGILENT TECHNOLOGIES INC | Methods for construction of pharmamers, i.e., vaccine components characterized by their multimerization domain and the attached biologically active molecules, and their use in preparation of vaccines that contains the pharmamers alone or in combination with other molecules | [94] |
WO 2005/018530 A2 | 20/08/2004 | Penetrating pharmaceutical foam | FOAMIX LTD | Alcohol-free cosmetic or pharmaceutical foam composition comprising water, a hydrophobic solvent, a surface-active agent, a gelling agent, an active component selected from the group of urea, hydroxy acid and a therapeutic enhancer and a propellant. The foam further comprises active agents and excipients with therapeutic properties having enhanced skin penetration | [95] |
US 8 668 937 B2 | 17/03/2012 | Topical nitric oxide systems and methods of use thereof | TRANSDERMAL BIOTECHNOLOGY INC | Compositions for delivery of nitric oxide, transdermally and/or to a mucosal surface | [96] |
US 2017 / 0232115 A1 | 12/10/2012 | Porous nanoparticle-supported lipid bilayers (protocells) for targeted delivery including transdermal delivery of cargo and methods thereof | SANDIA CORP | The protocells enhance SC permeability and enable transdermal delivery of active ingredients including macromolecules | [97] |
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