• These copolymers, in which the core is connected to PEG through a polyfunctional molecule such as citric, mucic, or tartaric acid, may be used to form nanoparticles for drug delivery applications. (biu.ac.il)
  • Tamoxifen-loaded poly(L-lactide) nanoparticles: development, characterization and in vitro evaluation of cytotoxicity. (springer.com)
  • Paper I: deals with the simplification of functional characterization for nanoparticles intended for use in biomedicine. (diva-portal.org)
  • There are currently two types of lipid nanoparticles, solid lipid nanoparticles (SLN) developed with saturated lipids and nanostructured lipid carriers (NLC) composed of both saturated and unsaturated lipids. (fortunepublish.com)
  • This study focuses on the preparation and characterization of biopolymeric alginate and chitosan nanoparticles for encapsulating the antidepressant drug Venlafaxine XR and analyzing it as an effective drug carrier and delivery system. (ijpsr.com)
  • 9. Agnihotri S. A., Mallikarjuna N. N., and Aminabhavi T. M., Recent Advances on Chitosan-based Micro-and Nanoparticles in Drug Delivery, Journal of Controlled Release, 100, 5-28, 2004. (irdpt.ir)
  • Lipid nanoparticles with a solid matrix (SLN, NLC, LDC) for oral drug delivery. (uns.ac.id)
  • Lipid Nanoparticles (Solid Lipid Nanopartocles and Nanostructured Lipid Carriers) for cosmetic, Dermal, and Transdermal Aplication. (uns.ac.id)
  • Kovachev P. Functionalization and Polymer Coating - Strategies to improve Drug Delivery from Mesoporous Silica Nanoparticles. (rjptonline.org)
  • Cisplatin-loaded chitosan microspheres were prepared by emulsification and ionotropic gelation method, and characterized for drug content, particle size, densities, flow properties, moisture content, and surface topography by SEM and in vitro drug release was evaluated in simulated lung fluid at 37 0 at pH 7.4. (ijpsonline.com)
  • In the present study, chitosan-loaded cisplatin microspheres were prepared and evaluated for dry powder inhalation delivery of cisplatin for local action of the drug in lungs, and thereby achieve improved therapy in lung cancer. (ijpsonline.com)
  • 11. Berthold A., Cremer K., and Kreuter J. S. T. P., Preparation and Characterization of Chitosan Microspheres as Drug Carrier for Prednisolone Sodium Phosphate as Model for Anti-inflammatory Drugs, Journal of Controlled Release , 39, 17-25, 1996. (irdpt.ir)
  • As the carrier of water-insoluble drugs, microspheres can play a role in increasing solubility and delaying releasing essence. (bvsalud.org)
  • Due to the extended experience of Nawah drug delivery team, in addition to the availability of all needed equipment for synthesis, formulation and characterization of Nano-drug delivery systems (NDDSs), we are happy to assist you in preparing your nanoformulation for research or R&D work. (nawah-scientific.com)
  • The solid phase synthesis of the crosslinkers, preparation of the particles by inverse microemulsion polymerization, HSP-triggered release of pSS and inactivation of HIV-1 studies are described. (nih.gov)
  • The synthesis of some types of silicate carriers is a method for improving the loading of the particles with active substances is confirmed. (rjptonline.org)
  • Download Polysaccharide Carriers for Drug Delivery or Read Polysaccharide Carriers for Drug Delivery online books in PDF, EPUB and Mobi Format. (tactilebook.net)
  • Click Download or Read Online Button to get Access Polysaccharide Carriers for Drug Delivery ebook. (tactilebook.net)
  • In order to Download Polysaccharide Carriers for Drug Delivery or Read Polysaccharide Carriers for Drug Delivery book, you need to create an account. (tactilebook.net)
  • Polysaccharide Carriers for Drug Delivery presents the latest information on the selection of safe materials. (tactilebook.net)
  • Such smart drug vectors can be self-assembled from peptides, which feature an excellent biocompatibility and, in particular, are straightforward to tune and optimize by changing the amino acid sequence. (uu.nl)
  • This book discusses various fundamental aspects of polysaccharide based nano-biocarrier drug delivery systems and its application in the delivery of small molecules, proteins, peptides, oligonucleotides and genes. (tactilebook.net)
  • Shakeel, F. Potential of solid dispersions to enhance solubility, bioavailability, and therapeutic efficacy of poorly water-soluble drugs: Newer formulation techniques, current marketed scenario and patents. (eurekaselect.com)
  • Poor oral bioavailability of BCS class 4 drug is due to poor aqueous solubility and poor permeability across intestine. (omicsonline.org)
  • Two factors govern the total oral absorption of drug i.e. drug's solubility and permeability across intestine. (omicsonline.org)
  • Solid Dispersion: Methods and Polymers to increase the solubility of poorly soluble drugs. (isca.me)
  • Potential of nanomedicines to overcome resistance, ameliorate solubility, improve pharmacological profile, and reduce adverse effects of chemotherapeutical drugs is thus highly regarded. (oaepublish.com)
  • Nanotechnology-based drug delivery systems are able to incorporate drugs or gene products with active anti-cancer activity but poor solubility, low bioavailability, or inadequate toxicological profile. (oaepublish.com)
  • Nano-drug delivery systems (NDDSs) are a class of nanomaterials that have abilities to increase the stability and water solubility of drugs, prolong the cycle time, increase the uptake rate of target cells or tissues, and reduce enzyme degradation, thereby improve the safety and effectiveness of drugs. (nawah-scientific.com)
  • The saturated solubility and mean dissolution time, in the case of F8 and F12, were significantly higher than the coarse drug powder. (dovepress.com)
  • Hence, poor aqueous solubility has become the leading hurdle for formulation, and scientists are concerned in improving oral delivery of insoluble drug candidates. (dovepress.com)
  • 1 - 3 Various approaches have been utilized for the enhancement of solubility and dissolution rate of poorly soluble drugs such as solid dispersions preparation, 4 inclusion in cyclodextrins, 5 and particle size (PS) reduction. (dovepress.com)
  • 6 Although these approaches improved solubility and dissolution of poorly soluble drugs, their commercial use is limited due to stability issues of the amorphous nature of the produced drug. (dovepress.com)
  • Nowadays, crystalline nanosuspensions (nanocrystals) are considered a valuable formulation for drugs that have a poor dissolution rate and/or aqueous solubility. (dovepress.com)
  • Upon loading sparingly soluble drugs, an improvement in their solubility was found, most likely by amorphization, obtained after crystallization of the problem substance in the delicate pores of these specific carriers. (rjptonline.org)
  • Amphiphilic core cross-linked star polymers as water-soluble, biocompatible and biodegradable unimolecular carriers for hydrophobic drugs, Polym. (jenkem.com)
  • 2. Popova T. Voycheva Ch. Tzankov B. Study on the influence of technological factors on drug loading of poorly water-soluble drug on MCM-41 mesoporous carrier. (rjptonline.org)
  • Proniosomes are water-soluble carrier particles that are coated with surfactant so these are dry formulations. (innovareacademics.in)
  • Preparation and characterization of ibuprofen loaded transferosome as a novel carrier for transdermal drug delivery system. (isca.me)
  • Formulation and evaluation of transdermal drug delivery system of clopidogrel bisulfate. (isca.me)
  • A review on: proniosomes-A surrogate carrier for improved transdermal drug delivery system. (innovareacademics.in)
  • Nanogels have been explored as drug delivery systems due to their advantageous properties, such as biocompatibility, high stability, tunable particle size, drug loading capacity, and possible modification of the surface for active targeting by attaching ligands that recognize cognate receptors on the target cells or tissues. (sharif.edu)
  • The APIMF procedure is one of four ways to provide information on the preparation control and stability of an API intended for use in a prequalified finished pharmaceutical product (FPP). (who.int)
  • Objectives: Although there is a high need for new drug molecules, most scientists focus on the advancement of novel pharmaceutical formulations since the present excipients lack important properties such as low release rate leading to repeated dosing. (eurekaselect.com)
  • Aside from this, pharmaceutical technologists aim to develop drug formulations that can target specific organs and tissues, lowering the possibility of adverse effects. (eurekaselect.com)
  • Prepared formulations were also evaluated for % drug permeation using non-everted rat intestinal sac method which showed that Pluronic was not involved in permeability enhancement of Cefixime. (omicsonline.org)
  • Controlled drug delivery systems, which are intended to deliver drugs at predetermined rates for predefined periods of time, have been used to overcome the shortcomings of conventional drug formulations. (scialert.net)
  • 6. Al Sagheer F. A., Al-Sughayer M. A., Muslim S., and Elsabee M. Z., Extraction and Characterization of Chitin and Chitosan from Marine Sources in Arabian Gulf, Carbohydrate Polymers, 77, 410-419, 2009. (irdpt.ir)
  • Natural Polysaccharides in Drug Delivery and Biomedical Applications provides a fundamental overview of natural polysaccharides, their sources, extraction methodologies, and characterizations. (tactilebook.net)
  • Liposomes act as drug carriers for entrapment of hydrophilic and hydrophobic drugs. (benthamscience.com)
  • Methods: Sitagliptin liposomes were prepared by the ethanol injection method and were evaluated for various physicochemical properties such as visual appearance, particle size distribution, zeta potential, % drug entrapment efficiency, % drug loading capacity and in vitro drug release studies. (benthamscience.com)
  • Entrapment of the drug venlafaxine XR is also significant because depression is nowadays becoming a mojor problem among the population. (ijpsr.com)
  • This review focuses on different aspects of proniosomes such as preparation, characterization, in vitro drug release, entrapment efficiency, applications in the present scenario in the market and future trends. (innovareacademics.in)
  • Moreover, a majority of chemotherapeutic drugs are highly hydrophobic and need to be diluted in organic solvents, which cause high toxicity, in order to reach effective therapeutic dose. (oaepublish.com)
  • Also, many effective chemotherapeutic drugs are hydrophobic and need to be diluted in an organic solvent (DMSO, Cremophor EL, ethanol etc .) that causes toxicity when injected. (oaepublish.com)
  • Design, preparation and characterization of cyclic RGDfK peptide modified poly (ethylene glycol)-block-poly (lactic acid) micelle for targeted delivery, Materials Science and Engineering: C, 2016. (jenkem.com)
  • It consisted in a post-synthetic cysteineS-alkylation reaction performed on cyclic sulfamidates and allowed the preparation of different lanthipeptides. (cnr.it)
  • Karakteristik kritis nano-structured lipid carrier (NLC) sangat dipengaruhi oleh komponen lipid padat dan lipid cair dalam sistem. (uns.ac.id)
  • 2016). Nano structured Lipid Carrier Based Drug Delivery System. (uns.ac.id)
  • Such nano-scale drug delivery systems need to be smart and tunable materials, since many hurdles have to be overcome to get a drug into cell (Figure 1). (uu.nl)
  • Polymer nano particles bind efficiently to the drug and disperse the drug proficiently into the system. (ijpsr.com)
  • Quantification of the drugs in a nano scale improves the dispersal and absorption rate of the drug. (ijpsr.com)
  • 2017). Nanostructured Lipid Carriers (NLCs): A Novel Based Nano Carrier for Drug Delivery and Drug Targeting. (uns.ac.id)
  • Efficient and targeted drug/siRNA co-delivery mediated by reversibly crosslinked polymersomes toward anti-inflammatory treatment of ulcerative colitis (UC), Nano Research, 2019, 1-9. (jenkem.com)
  • Magnetic nano/micro-particles based on clinoptilolite-type of natural zeolite (CZ) were fabricated and were expected to act as carriers for controlled drug delivery/release, imaging and local heating in biological systems. (nature.com)
  • These techniques are particularly suitable for developing environmentally sustainable and energy-efficient synthetic process to prepare biopolymer-based nano-sized material to be employed as drug delivery carrier systems. (cnr.it)
  • Giddi HS, Arunagirinathan MA, Bellare JR. Self-assembled surfactant nano-structures important in drug delivery: a review. (innovareacademics.in)
  • Consequently, they accomplished the preparation of a platform with chemically active sites and the development of biohybrid devices capable of converting energy of biomolecular motors into useful work. (wikipedia.org)
  • Methods: This review aims to cover the different polymer-based gel types, the development and characterization methods, as well as applications thereof. (eurekaselect.com)
  • Pokharkar, B.V. Development and characterization of liposomal drug delivery system for nimesulide. (benthamscience.com)
  • Drug Development and Industrial Pharmacy , 20 (4), 535-546. (tmu.edu.tw)
  • The aim of this work was the development of nanostructured lipid carriers (NLC) using conventional fats and oils (soybean oil, SO and fully hydrogenated soybean oil, FHSO) for incorporation of free phytosterols (FP). (fortunepublish.com)
  • In addition, the controlled drug delivery area needs further development of techniques for delivery of peptide and protein drugs. (scialert.net)
  • Enhanced delivery of bioactive molecules through the skin and cellular membranes by means of an ethosomal carrier opens numerous challenges and opportunities for the research and future development of novel improved therapies. (ajptonline.com)
  • Hence, a major goal in cancer drug development and therapy is to increase tumor-specific drug uptake while reducing uptake into normal tissues to minimize toxicities. (aspetjournals.org)
  • 9. Popova T. Tzankov B. Voycheva C. Yoncheva K. Lambov N. Development of advanced drug delivery systems with bicalutamide based on mesoporous silica particles. (rjptonline.org)
  • In the development of new dosage forms, drug delivery using nanotechnology is playing a vital role. (innovareacademics.in)
  • Studies of drug release from polymeric systems containing multiblock copolymers and studies of polymer degradation were also performed. (biu.ac.il)
  • Khalili, S. Polymeric nanocarriers in targeted drug delivery systems: A review. (eurekaselect.com)
  • Formulation and evaluation of gliptin loaded polymeric nanomicelles for controlled drug delivery. (benthamscience.com)
  • Aceclofenac topical dosage forms: in vitro and in vivo characterization. (isca.me)
  • Therefore, developing a drug delivery system that optimizes the pharmaceutical action of a drug while reducing its toxic side effects in vivo is a challenging task. (ijpsr.com)
  • Kolev I. Mihály J. Tzankov B. Momekov G. Lambov N. Yoncheva K. Carboxylic modified spherical mesoporous silicas аs drug delivery carriers International Journal of Pharmaceutics. (rjptonline.org)
  • Nanosuspensions consist of stabilized submicron sized crystalline drug particles in liquid medium, usually water. (dovepress.com)
  • The mesoporous silica particles (MSNs) have been investigated as potential drug delivery carriers. (rjptonline.org)
  • Therefore, the mesoporous structure of CZ particles provided a unique platform for preparation of multifunctional magnetic and optical probes suitable for optical imaging, MRI, thermo- and phototherapy and as effective containers for controlled drug delivery. (nature.com)
  • Thus, drug release from devices made from these polymers will display release rates that are pH sensitive. (scialert.net)
  • Liposomes serve as promising active carriers of drugs to posterior segment eye disorders due to improvement in intravitreal half-life and targeted sustained drug delivery to the retina. (benthamscience.com)
  • Recent applications of liposomes in ophthalmic drug delivery. (benthamscience.com)
  • study deformable liposomes as potential carriers for transdermal drug delivery. (ddw-online.com)
  • The system is having donar and receiver compartment for studying permeation of drug across the membrane. (omicsonline.org)
  • Comparative study was carried out using Pluronic as solid dispersion and beta cyclodextrin as inclusion complexation in different drug to polymer ratios through physical mix, kneading, solvent evaporation and spray drying technique. (omicsonline.org)
  • Preparation and characterization of stearic acid nanostructured lipid carriers by solvent diffusion method in an aqueous system. (uns.ac.id)
  • Her predominant symptoms, such as sore throat and earache, improved after antimicrobial drug therapy, and she recovered quickly. (cdc.gov)
  • Antimicrobial drug susceptibility testing of the 3 isolates was performed on Mueller-Hinton blood agar (supplemented with 5% sheep blood) by using the Etest system after overnight incubation at 37°C and in 5% CO 2 . (cdc.gov)
  • The strains were tested for antimicrobial drug susceptibility, produc- tion of -lactamases, and presence of mec A by PCR ( 5 ). (cdc.gov)
  • 2020 Feature in the exhibit Científiques Catalanes 2.0 2017 Anna Roig, ALBUS: Albumin Award Program from Grifols Scientific Awards UAB Best PhD thesis award to six thesis that I have supervised or co supervised (Lluis Casas, Martí Gich, Elena Taboada, Elisa Carenza, Nerea Murillo, Laura González Moragas) 2015 Elisa Carenza, I Prize Dr. Ramon Ríos, Fundación Foltra 2014 'Los Nuevos Materiales en el Aula' I Prize Reach.Out! (icmab.es)
  • How could Poly Glycerol Sebacate be utilized as a Drug Delivery System more efficient? (icbcongress.com)
  • Poly(ethylene glycol)-block-poly(d,l-lactide acid) micelles anchored with angiopep-2 for brain-targeting delivery, Journal of Drug Targeting, 2011, 19:3. (jenkem.com)
  • However, to precisely steer and program the biophysical and pharmaceutical profile of peptide-based drug vectors, a precise knowledge of their supramolecular code is mandatory. (uu.nl)
  • We have recently shown [1] that the integration of solid-state NMR with multi-scale molecular dynamics simulations gives access to high-resolution structures of supramolecular peptide-based drug vectors (Figure 2). (uu.nl)
  • In the proposed master project, the student will investigate the supramolecular structure and dynamics of a peptide-based drug vector for gene therapy. (uu.nl)
  • This review encompasses the significant recent advancements in drug delivery as well as molecular imaging and diagnosis of cancer exploiting polymer-based, lipid-based and inorganic nanoparticulate systems. (eurekaselect.com)
  • Review on: niosomes-targeted and controlled drug delivery novel carrier system, C.B.S [publication]. (innovareacademics.in)
  • Çalış, S. Novel advances in targeted drug delivery. (eurekaselect.com)
  • Although, significant progress has been made in the controlled drug delivery area, more advances are yet to be made for treating many clinical disorders, such as diabetes and rhythmic heart disorders. (scialert.net)
  • In passive mechanism, diffusion of drug through close junctions of epithelial cells occurs depending on its size and charge while in active transport, uptake of drug is mediated by carrier i.e. active proteins [ 3 - 5 ]. (omicsonline.org)
  • L-3 followed Korsmeyer- Peppas model with fickian diffusion transport of drug release giving n' (0.3094), r2 (0.9753), with 83.78 ± 0.97% of sustained drug release. (benthamscience.com)
  • I am a materials scientist working in the preparation, characterization and new uses of functional nanomaterials. (icmab.es)
  • Among the vesicular carriers, proniosomes are superior. (innovareacademics.in)
  • Proniosomes prolong the existence of the drug in the systemic circulation and finally reduces toxicity. (innovareacademics.in)
  • Rao R, Kakar R, Anju G, Sanju N. Review on proniosomes: an emerging vesicular system in drug delivery and cosmetics. (innovareacademics.in)
  • Sadanandan A, Boby Johns G, Samuel J, Raj P, Thomas N, Daisy PA, Carla B. A review on: proniosomes-An innovative approach to vesicular drug delivery system. (innovareacademics.in)
  • Akhilesh D, Hazel G, Kamath J. Proniosomes-A propitious provesicular drug carrier. (innovareacademics.in)
  • Sudhamani T, Priyadarisini N, Radhakrishnan M. A review on: proniosomes-A promising drug carrier. (innovareacademics.in)
  • Akhilesh D, Faishal G, Kamath J. Comparative study of carriers used in proniosomes. (innovareacademics.in)
  • Review on: proniosomes-A propitious provesicular drug carrier. (innovareacademics.in)
  • A review on proniosomes: a key to improved drug delivery. (innovareacademics.in)
  • The pioneers of this field, ahead of their time, were Montemagno and Bachand with a 1999 work regarding specific attachment strategies of biological molecules to nanofabricated substrates enabling the preparation of hybrid inorganic/organic nanoelectromechanical systems, so called NEMS. (wikipedia.org)
  • Because of their unique structure, ethosomes are able to encapsulate and deliver through the skin highly lipophilic molecules such as cannabinoids, testosterone, and minoxidil, as well as cationic drugs such as propranolol, trihexyphenidil, Cyclosporine A, insulin, Salbutamol etc. (ajptonline.com)
  • Lipid-based nanoparticle (LBNP) systems represent one of the most promising colloidal carriers for bioactive organic molecules. (mdpi.com)
  • They make it possible to create bonds or interactions between the drug molecules and the carrier. (rjptonline.org)
  • Once in the cell interior smart drug carriers need to be sensitive to a stimulus that triggers the release of the drug. (uu.nl)
  • If symptoms of a disease display circadian variation, drug release should also vary over time. (scialert.net)
  • PSDDS wherein the drug release is controlled primarily by the delivery system, stimuli induced PSDDS in which release is controlled by the stimuli, such as the pH present in the intestinal tract. (scialert.net)
  • It would be highly beneficial if the active agents were delivered by a system that sensed the signal caused by disease, judged the magnitude of signal and then acted to release the right amount of drug in response. (scialert.net)
  • The pH range of fluids in various segments of the gastrointestinal tract may provide environmental stimuli for responsive drug release. (scialert.net)
  • Tablets were formulated of selected batches and evaluated for drug release and physical parameters. (sld.cu)
  • Prolonged (upto 5 h) and slow drug release was observed with resin 214 at higher concentration. (sld.cu)
  • out of three resins chosen, Indion ® 214 at higher concentration exhibit excellent taste masking as well as sustained drug release action. (sld.cu)
  • This paper describes the design, construction and characterization of the first anti-HIV drug delivery system that is triggered to release its contents in the presence of human semen. (nih.gov)
  • Comparative genome analysis and characterization of the Salmonella Typhimurium strain CCRJ_26 isolated from swine carcasses using whole-genome sequencing approach. (cdc.gov)
  • Mishra A, Kapoor A, Bhargava S. A review on: proniosomal gel as a carrier for improved transdermal drug delivery. (innovareacademics.in)
  • It is for example imaginable to design a drug vector that only releases its cargo once it feels the acidic environment of a tumor cell. (uu.nl)
  • With the atomic level data, the student will rationally design the biophysical profile (such as drug binding & retention) of the carrier. (uu.nl)
  • Drug delivery is the most essential feature in drug administration facility and the design of Nanosystems makes the action more consistent an appropriate. (ijpsr.com)
  • Lungs provide a large surface area and hence can be explored as a potential site for the systemic delivery of drugs. (ijpsonline.com)
  • Aras, O., Kazanci, M. - Production of collagen micro- and nanofibers for potential drug-carrier systems, Journal of Enzyme Inhibition and Medicinal Chemistry 30 (6) (2015) 1013-1016. (ac.vn)
  • The efficacy of many drugs is often limited by their potential to reach the site of therapeutic action. (ijpsr.com)
  • This article reviews various aspect of ethosomes including their preparation, characterization, potential advantages and their applications in drug delivery. (ajptonline.com)
  • According to the chemical characterization and physicochemical properties studied, the extracted pectin from watermelon rind would have a high potential to be used in food industry. (hindawi.com)
  • In most cases (conventional dosage forms), only a small amount of administered dose reaches the target site, while the majority of the drug distributes throughout the rest of the body in accordance with its physicochemical and biochemical properties. (ijpsr.com)
  • The first step in oral absorption of solid dosage forms is dissolution of drug compound in the gastrointestinal lumen contents. (dovepress.com)
  • Title: Optimizing colonoscopy preparation: the role of dosage, timing and diet. (aablocks.com)
  • They described the production of large amounts of F1-ATPase from the thermophilic bacteria Bacillus PS3 for the preparation of F1-ATPase biomolecular motors immobilized on a nanoarray pattern of gold, copper or nickel produced by electron beam lithography. (wikipedia.org)
  • Klebsiella pneumoniae as a key trafficker of drug resistance genes from environmental to clinically important bacteria. (cdc.gov)
  • Present work was undertaken to increase oral bioavailability of BCS class 4 drug i.e. (omicsonline.org)
  • Another prospective porous material is zeolite, which shares many of the favorable properties of silica, especially in biomedical applications related to transportation of low molecular weight drugs and imaging agents. (nature.com)
  • Nanomaterials have demonstrated a wide range of applications and recently, novel biomedical studies are devoted to improving the functionality and effectivity of traditional and unmodified systems, either drug carriers and common scaffolds for tissue engineering or advanced hydrogels for wound healing purposes. (researchgate.net)
  • Nowadays targeted drug delivery, as well as the early cancer diagnosis is a key research area where nanomedicine is playing a crucial role. (eurekaselect.com)
  • For usual absorption of drug it is soluble then it will reach intestinal wall in dissolved state and later absorbed in gut membranes combining all above transport mechanisms. (omicsonline.org)
  • Ethosomes are noninvasive delivery carriers that enable drugs to reach the deep skin layers and/or the systemic circulation. (ajptonline.com)
  • Efficacious drug deposition in the target site and operated activation of therapeutic and imaging agents reduce treatment time, while avoiding adverse damage and side effects resulting from systemic administration. (nature.com)
  • 1 Drug Delivery and Targeting Group, Molecular Biology and Biochemistry Research Centre for Nanomedicine (CIBBIM-Nanomedicine), Vall d'Hebron Institut de Recerca, Universitat Autònoma de Barcelona , Barcelona 08035, Spain . (oaepublish.com)