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4th Annual Congress on Nanomedicine and Drug Delivery, will be organized around the theme “Manifesting advancements in the field of Nanomedicine and Drug Delivery”

Nanodelivery Congress 2019 is comprised of keynote and speakers sessions on latest cutting edge research designed to offer comprehensive global discussions that address current issues in Nanodelivery Congress 2019

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 Advanced Nanomedicine is simply the nanotechnology applications in a healthcare setting and the majority of benefits that have already been seen involve the use of nanoparticles to improve the behaviour of drug substances and in drug delivery. Today, nanomedicines are used globally to improve the treatments and lives of patients suffering from a range of disorders including ovarian and breast cancer, kidney disease, fungal infections, elevated cholesterol, menopausal symptoms, multiple sclerosis, chronic pain, asthma and emphysema. Nanomedicine has the potential to develop radical new therapies based on an unprecedented control over both intracellular processes and the extracellular environment at the nanometer scale. To create precise solutions for intricate medical challenges in the area of wound healing, tissue regeneration and mitochondrial disease physical scientists, medical doctors, and industrial partners, work closely in the Radboud Nanomedicine Alliance. The National Nanotechnology Initiative expects new commercial applications in the pharmaceutical industry that may include advanced drug delivery systems, new therapies, and in vivo imaging.

Personalizedmedicine aims to individualize chemotherapeutic interventions on the basis of ex vivo and in vivo information on patient- and disease-specific characteristics. By noninvasively visualizing how well image-guided nanomedicines-that is, submicrometer-sized drug delivery systems containing both drugs and imaging agents within a single formulation of drug, and designed to more specifically deliver drug molecules to pathologic sites-accumulate at the target site, patients likely to respond to nanomedicine-based therapeutic interventions may be preselected. In addition, by longitudinally monitoring how well patients respond to nanomedicine-based therapeutic interventions, drug doses and treatment protocols can be individualized and optimized during follow-up. Furthermore, noninvasive imaging information on the accumulation of nanomedicine formulations in potentially endangered healthy tissues may be used to exclude patients from further treatment. Consequently, combining noninvasive imaging with tumor-targeted drug delivery seems to hold significant potential for personalizing nanomedicine-based chemotherapy interventions, to achieve delivery of the right drug to the right location in the right patient at the right time.

The Novel Drug Delivery Systems are the method by which a drug is delivered can have a significant effect on its efficacy. Some drugs have an optimum concentration range within which maximum benefit is derived, and concentrations above or below this range can be toxic or produce no Local Drug Delivery Systems benefit at all. On the other hand, the very slow progress in the efficacy of the treatment of severe diseases, has suggested a growing need for a multidisciplinary approach to the delivery of therapeutics to targets in tissues. From this, new ideas on controlling the pharmacokinetics, pharmacodynamics, non-specific toxicity, immunogenicity, bio recognition, and efficacy of drugs were generated. These new strategies, often called drug delivery systems (DDS), are based on interdisciplinary approaches that combine polymer science, pharmaceutics, bio conjugate chemistry, and molecular biology. On the other hand, this reference discusses advances in the design, optimization, and adaptation of gene delivery systems for the treatment of cancer, cardiovascular, pulmonary, genetic, and infectious diseases, and considers assessment and review procedures involved in the development of gene-based pharmaceuticals.

The most encouraging utilization of nanomaterials is the guarantee of focused, site-particular medication delivery. The capability of taking out a tumorous outgrowth with no inadvertent blow-back through nanomaterial-based medication delivery has made noteworthy intrigue and nanoparticles shape the reason for bio-nano-materials and real endeavors in planning drug delivery frameworks depend on functionalized nanoparticles. At first, they were contrived as bearers for immunizations and anticancer medications and after that the nanometer measure extents may altogether improve the medication delivery by influencing the bio-dissemination and toxicodynamics of medications. This can make in vivo delivery of numerous sorts of medications which present genuine delivery issues, a generally simple errand. Changing or functionalizing nanoparticles to convey tranquilizes through the blood cerebrum obstruction for focusing on mind tumors can be viewed as a splendid result of this innovation. They can infiltrate profound into tissues and are consumed by the cells proficiently. Nanoparticles have extended the extent of pharmacokinetics for insoluble medications.

 

Advances which can improve solubility, bioavailability, stability, scalability and ability to manufacture.

 

RP Scherer Softgel Delivery Technologies

Zydis® Fast Dissolve Delivery Technology

OptiPact™ Roller Compaction

Inhalation

Fluid-bed Processing

Liquid & Sterile formulation and development

 

Nano engineered drug delivery systems as an effective system to defeat constraints associated with antibiotic drug therapy. Anti-infection agents epitomized into nanodelivery systems will add to enhanced administration of patients with different irresistible maladies and to beating the genuine worldwide weight of anti-microbial opposition. A broad audit of a few anti-microbial stacked nanocarriers that have been defined to target medications to irresistible destinations, accomplish controlled medication discharge profiles, and address definition challenges, for example, low-tranquilize ensnarement efficiencies, poor dissolvability and steadiness is exhibited in this paper. The physicochemical properties and the in vitro/in vivo exhibitions of different anti-toxin stacked conveyance frameworks, for example, polymeric nanoparticles, micelles, dendrimers, liposomes, strong lipid nanoparticles, lipid– polymer cross breed nanoparticles, nanohybirds, nanofibers/platforms, nanosheets, nanoplexes, and nanotubes/horn/bars and nanoemulsions, are featured and assessed.

 

Biomaterials zone look to create novel materials and apply known materials to test fundamental logical speculations over different length scales. Macroscale biomaterials are utilized to create tissue regenerative methodologies (e.g., to advance injury recuperating) and furthermore to think about the effect of the structure and physical properties of three-dimensional builds on cell conduct. Microscale delivery systems are commonly used as Scaffolddepots for privately supported, smart medication conveyance. At long last, critical spotlight is on materials of the nanoscale measurement, especially for applications in medication and quality conveyance. In the medication conveyance zone, nanomaterials are created for applications, for example, focusing of existing treatments to make them more protected and successful, empowering the helpful utilization of new classes of biologics that have noteworthy pharmacokinetic obstructions without conveyance advances, and improvement of new treatments for adjustment of the invulnerable framework. Novel medication delivery advances are being created for applications crosswise over numerous illness application regions, with specific spotlight on the zone of new treatments that can square tumor improvement and metastasis.

 

Nanomedicines in Theranostics are advantageous over standard low-molecular-weight drugs in several different regards. They reduce renal excretion and/or hepatic degradation, leading to prolonged circulation times, reduce the volume of distribution, leading to less accumulation in healthy non-target tissues (‘site-avoidance drug delivery’), improve the ability of drugs to accumulate at pathological sites (‘site-specific drug delivery’) and improve the therapeutic index of drugs, by increasing their accumulation at the target site and/or reducing their localization in potentially endangered healthy organs. In addition, nanomedicine formulations assist low-molecular-weight (chemo-) therapeutic agents in overcoming several additional barriers to efficient drug delivery to pathological sites. We show that theranostic nanomedicines are highly suitable systems for monitoring drug delivery, drug release and drug efficacy. The (pre)clinically most relevant applications of theranostic nanomedicines relate to their use for validating and optimizing the properties of drug delivery systems, and to their ability to be used for pre-screening patients and enabling personalized medicine.

This zone manages the repair or substitution of ailing or harmed tissues and organs by applying strategies from quality treatment, cell treatment, the measurements of bioactive atoms and tissue building, by invigorating repair systems of the claim body. The creation of new materials and emotionally supportive networks, the utilization of undifferentiated organisms (grown-up, embryonic and iPS) and the generation of particles and biomimetic peptides which fill in as signs for cell bond and separation are the principle focal points of this territory. The general research lines inside this zone are Molecular and cell functionalisation of biomaterials for the making of tissue designing items, Biocompatibility and harmfulness of implantable gadgets, Cellular and atomic systems ensnared in the recovery of organs and tissues.

 

  • Track 9-1Dental regeneration
  • Track 9-2Skin regeneration
  • Track 9-3Nanostructured scaffolds
  • Track 9-4Nanoparticles-based skin regeneration
  • Track 9-5Stem cell-based skin regeneration
  • Track 9-6Cartilage regeneration
  • Track 9-7Nerve regeneration
  • Track 9-8Myocardial regeneration
  • Track 9-9Ocular regeneration
  • Track 9-10Hepatic regeneration
  • Track 9-11Bone tissue regeneration

Incorporating nanoparticles for pharmaceutical purposes, for example, tranquilize planning should be possible in two techniques. Base up process, for example, pyrolysis, idle gas buildup, solvothermal response, sol-gel creation and organized media in which hydrophobic compound, for example, liposomes are utilized as bases to mount the medication. Top down process, for example, weakening/processing in which the medication is etched down to frame a nanoparticle.

 

They are different nanomedicine treatment procedures to coordinate treatment straightforwardly to ailing cells, limiting the harm to solid tissue that happen in current techniques, for example, radiation treatment cause. Particles are designed with the goal that they are pulled in to sick cells, which permits coordinate treatment of those cells. This method diminishes harm to sound cells in the body. Nanofibers can empower the generation of ligament in harmed joints. Nanoparticles, when initiated by x-beams, that create electrons that reason the devastation of malignancy cells to which they have connected themselves. This is proposed to be utilized instead of radiation treatment with substantially less harm to solid tissue. Attractive nanoparticles that connect to disease cells in the circulatory system may enable the malignancy cells to be expelled before they set up new tumors. A technique to make radiation treatment more impact in battling prostate growth is utilizing radioactive gold nanoparticles appended to an atom that is pulled in to prostate tumor cells.

 

The ongoing rise of "Molecular imaging" as an incorporated control in scholastic therapeutic focuses has set the phase for a transformative jump in demonstrative imaging and therapy. Molecular imaging is anything but a substitute for the customary procedure of picture arrangement and understanding, however is expected to enhance analytic precision and affectability by giving an in vivo simple of immunocytochemistry or in situ hybridization. To show such nanosystems, a couple of models of MRI and ultrasound applications in atomic imaging are refered to. Paramagnetic polymerized liposomes bearing immune response ligands to neovascular integrins αvβ3 have been utilized for focusing on trial tumor angiogenesis, and amassing following 24 hours permits adequate flag for imaging. Similarly, fluid perfluorocarbon nanoparticle emulsions focused to αvβ3 likewise allow vigorous tumor imaging after just 1 hour in the dissemination, with particular take-up exhibited by in vivo rivalry experiments. Indeed, fluid perfluorocarbon nanoparticles were the main case of sub-atomic focusing on specialists comprehensively helpful for MRI of thrombi by joining counter acting agent ligands coordinated against cross-connected fibrin, and they have been demonstrated as of late to empower portrayal of trial thrombi in vivo and human unsteady carotid plaques ex vivo.

 

The biomaterials and medication conveyance aggregate spotlights on the union, manufacture, and assessment of biomaterials, including nanomaterials for critical applications in biomedicine. Our exploration endeavors underscore the advancement of new or enhanced biomaterials with important physical, synthetic, and organic properties. These creative materials are misused for an assortment of innovations, including imaging contrast operators, tissue building platforms, sedate conveyance, and counterfeit infections for quality treatment. For instance, the controlled arrival of bioactive atoms, for example, peptides, proteins, and plasmids, are in effect effectively researched for the treatment of human maladies and additionally for regenerative drug.

 

Tissue engineering evolved from the field of biomaterials development and refers to the practice of combining scaffolds, cells, and biologically active molecules into functional tissues. The goal of tissue engineering is to assemble functional constructs that restore, maintain, or improve damaged tissues or whole organs. Artificial skin and cartilage are examples of engineered tissues that have been approved by the FDA; however, currently they have limited use in human patients. Tissue engineering plays a relatively small role in patient treatment.  Supplemental bladders, small arteries, skin grafts, cartilage, and even a full trachea have been implanted in patients, but the procedures are still experimental and very costly

  • Track 14-1Cartilage Tissue Engineering
  • Track 14-2Dental Tissue Engineering
  • Track 14-3Biomaterials Tissue Engineering
  • Track 14-4Bioreactors Tissue Engineering
  • Track 14-5Stem Cells Tissue Engineering
  • Track 14-6Genetic Tissue Engineering

Nanoparticle delivery systems are gaining traction in their clinical utility and are investigated for the delivery of chemotherapeutic drugs, siRNAs and other agents, and also as diagnostic and imaging applications. Physicochemical properties of nanoparticles play an important role in their biological performance. Nanoparticles of various sizes, shapes, elasticities, and surface chemistries are becoming more widely used; however, this presents a number of translational challenges from a materials point of view. Specifically, as nanoparticle delivery systems become more advanced, methods for their synthesis, scale-up, and characterization need to follow suit. Furthermore, as advancements in technology allow for precise control over all nanoparticle parameters, approaches to systematically analyze the effects these parameters have on nanoparticle performance are essential.

 

Nanomedicines have been in the forefront of pharmaceutical research in the last decades, creating new challenges for research community, industry, and regulators. There is a strong demand for the fast development of scientific and technological tools to address unmet medical needs, thus improving human health care and life quality. Tremendous advances in the biomaterials and nanotechnology fields have prompted their use as promising tools to overcome important drawbacks, mostly associated to the non-specific effects of conventional therapeutic approaches. However, the wide range of application of nanomedicines demands a profound knowledge and characterization of these complex products. Their properties need to be extensively understood to avoid unpredicted effects on patients, such as potential immune reactivity. Research policy and alliances have been bringing together scientists, regulators, industry, and, more frequently in recent years, patient representatives and patient advocacy institutions. In order to successfully enhance the development of new technologies, improved strategies for research-based corporate organizations, more integrated research tools dealing with appropriate translational requirements aiming at clinical development, and proactive regulatory policies are essential in the near future. This review focuses on the most important aspects currently recognized as key factors for the regulation of nanomedicines, discussing the efforts under development by industry and regulatory agencies to promote their translation into the market.