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1.
Article in English | MEDLINE | ID: mdl-32426338

ABSTRACT

The emerging field of theranostics for advanced healthcare has raised the demand for effective and safe delivery systems consisting of therapeutics and diagnostics agents in a single monarchy. This requires the development of multi-functional bio-polymeric systems for efficient image-guided therapeutics. This study reports the development of size-controlled (micro-to-nano) auto-fluorescent biopolymeric hydrogel particles of chitosan and hydroxyethyl cellulose (HEC) synthesized using water-in-oil emulsion polymerization technique. Sustainable resource linseed oil-based polyol is introduced as an element of hydrophobicity with an aim to facilitate their ability to traverse the blood-brain barrier (BBB). These nanogels are demonstrated to have salient features such as biocompatibility, stability, high cellular uptake by a variety of host cells, and ability to transmigrate across an in vitro BBB model. Interestingly, these unique nanogel particles exhibited auto-fluorescence at a wide range of wavelengths 450-780 nm on excitation at 405 nm whereas excitation at 710 nm gives emission at 810 nm. In conclusion, this study proposes the developed bio-polymeric fluorescent micro- and nano- gels as a potential theranostic tool for central nervous system (CNS) drug delivery and image-guided therapy.

2.
Drug Discov Today ; 23(7): 1436-1443, 2018 07.
Article in English | MEDLINE | ID: mdl-29775669

ABSTRACT

Hydrogel-based drug delivery systems (DDSs) have versatile applications such, as tissue engineering, scaffolds, drug delivery, and regenerative medicines. The drawback of higher size and poor stability in such DDSs are being addressed by developing nano-sized hydrogel particles, known as nanogels, to achieve the desired biocompatibility and encapsulation efficiency for better efficacy than conventional bulk hydrogels. In this review, we describe advances in the development of nanogels and their promotion as nanocarriers to deliver therapeutic agents to the central nervous system (CNS). We also discuss the challenges, possible solutions, and future prospects for the use of nanogel-based DDSs for CNS therapies.


Subject(s)
Central Nervous System Agents/administration & dosage , Drug Carriers , Nanomedicine/methods , Nanoparticles , Animals , Blood-Brain Barrier/metabolism , Capillary Permeability , Central Nervous System Agents/chemistry , Central Nervous System Agents/metabolism , Drug Compounding , Gels , Humans
3.
Gels ; 4(3)2018 Sep 06.
Article in English | MEDLINE | ID: mdl-30674851

ABSTRACT

The ongoing progress in the development of hydrogel technology has led to the emergence of materials with unique features and applications in medicine. The innovations behind the invention of nanocomposite hydrogels include new approaches towards synthesizing and modifying the hydrogels using diverse nanofillers synergistically with conventional polymeric hydrogel matrices. The present review focuses on the unique features of various important nanofillers used to develop nanocomposite hydrogels and the ongoing development of newly hydrogel systems designed using these nanofillers. This article gives an insight in the advancement of nanocomposite hydrogels for nanomedicine.

4.
Sci Rep ; 7: 45663, 2017 04 04.
Article in English | MEDLINE | ID: mdl-28374799

ABSTRACT

In this research, we demonstrate cell uptake of magneto-electric nanoparticles (MENPs) through nanoelectroporation (NEP) using alternating current (ac)-magnetic field stimulation. Uptake of MENPs was confirmed using focused-ion-beam assisted transmission electron microscopy (FIB-TEM) and validated by a numerical simulation model. The NEP was performed in microglial (MG) brain cells, which are highly sensitive for neuro-viral infection and were selected as target for nano-neuro-therapeutics. When the ac-magnetic field optimized (60 Oe at 1 kHz), MENPs were taken up by MG cells without affecting cell health (viability > 92%). FIB-TEM analysis of porated MG cells confirmed the non-agglomerated distribution of MENPs inside the cell and no loss of their elemental and crystalline characteristics. The presented NEP method can be adopted as a part of future nanotherapeutics and nanoneurosurgery strategies where a high uptake of a nanomedicine is required for effective and timely treatment of brain diseases.


Subject(s)
Brain/drug effects , Microglia/drug effects , Nanoparticles/chemistry , Cell Line , Drug Carriers , Electricity , Electroporation/methods , Humans , Magnetic Fields , Microscopy, Electron, Transmission/methods , Nanomedicine/methods
5.
Trends Biotechnol ; 35(4): 308-317, 2017 04.
Article in English | MEDLINE | ID: mdl-28277248

ABSTRACT

Health agencies have declared the recent Zika virus (ZIKV) infection an epidemic and a public health emergency of global concern due to its association with microcephaly and serious neurological disorders. The unavailability of effective drugs, vaccines, and diagnostic tools increases the demand for efficient analytical devices to detect ZIKV infection. However, high costs, longer diagnostic times, and stringent expertise requirements limit the utility of reverse transcriptase-PCR methods for rapid diagnostics. Therefore, developing portable, sensitive, selective, and cost-effective sensing systems to detect ZIKV at picomolar concentrations in biofluids would be a breakthrough in diagnostics and therapeutics. This paper highlights the advancements in developing smart sensing strategies to monitor ZIKV progression, with rapid point-of-care diagnostics as the ultimate aim.


Subject(s)
Biosensing Techniques , Electrochemical Techniques , Microfluidic Analytical Techniques , Zika Virus Infection , Aedes/virology , Animals , Early Diagnosis , Humans , Reverse Transcriptase Polymerase Chain Reaction , Zika Virus/genetics , Zika Virus/isolation & purification , Zika Virus Infection/diagnosis , Zika Virus Infection/transmission , Zika Virus Infection/virology
6.
Sci Rep ; 6: 25309, 2016 05 04.
Article in English | MEDLINE | ID: mdl-27143580

ABSTRACT

Least component-based delivery of drug-tagged-nanocarriers across blood-brain-barriers (BBB) will allow site-specific and on-demand release of therapeutics to prevent CNS diseases. We developed a non-invasive magnetically guided delivery of magneto-electric nanocarriers (MENCs), ~20 nm, 10 mg/kg, across BBB in C57Bl/J mice. Delivered MENCs were uniformly distributed inside the brain, and were non-toxic to brain and other major organs, such as kidney, lung, liver, and spleen, and did not affect hepatic, kidney and neurobehavioral functioning.


Subject(s)
Central Nervous System/chemistry , Drug Carriers/adverse effects , Drug Carriers/pharmacokinetics , Magnetic Fields , Metal Nanoparticles/adverse effects , Animals , Drug Carriers/administration & dosage , Metal Nanoparticles/administration & dosage , Mice, Inbred C57BL
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