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Patent Classification
Drug Delivery System, Solubilization
-
Use of
oligomers and polymers for drug solubilization, stabilization, and
delivery
-
Hybrid system for
solubilizing pharmaceutically active substances in polymer matrices
-
Peptides as solubilizing excipients for transforming growth factor beta
proteins
-
Water soluble nanoparticles of hydrophilic and hydrophobic active
materials and an apparatus and method for their production
-
Formulation solubilizing water-insoluble agents and preparation method
thereof
-
N,N-dinitramide salts as solubilizing agents for
biologically active agents
-
Composition for solubilizing salicylic acid
-
Water-soluble compositions of bioactive
lipophilic compounds
-
Solubilizers containing alk(en)yl oligoglycosides
and polyol components, and methods of solubilizing using the same
-
Compositions containing therapeutically active
components having enhanced solubility
-
Solvent
system for enhancing solubility
-
Process
for solubilizing pharmaceutically active ingredients in water and in
aqueous vehicles
-
Pharmaceutical composition comprising cyclosporin
-
Pharmaceutical
composition comprising cyclosporin
-
C7
-C12 Diol & Diol alkoxylates as coupling agents for
surfactant formulations
-
Method
of solubilizing itraconazole
-
Water-soluble
compositions of bioactive lipophilic compounds
-
Solubility
parameter based drug delivery system and method for altering drug
saturation concentration
-
Alkyl or olefinic endcapped polyalkylene oxide
solubilizer
-
Method
and compositions for solubilization and stabilization of polypeptides,
especially proteins
-
Aqueous composition containing solubilized or
dispersed oil-soluble substance
Drug Delivery System,
Solution/Supersaturated Solution
-
Retinoid solutions
and formulations made therefrom
-
Stable
bicarbonate-based solution in a single container
-
Preparation of aqueous
clear solution dosage forms with bile acids
-
Preparation of aqueous
clear solution dosage forms with bile acids
-
Liquid pharmaceutical composition
-
Pharmaceutical solutions of modafinil compounds
-
Homogeneous cyclosporin-containing solution
-
Aqueous pharmaceutical composition containing
moxifloxacin or salts thereof
-
IFN-.beta. liquid formulations
-
Stabilized aspirin compositions and method of preparation for oral and
topical use
-
Ionic aqueous composition containing levomenthol
-
Soluble contraceptive liquid formulation
-
Method
for preparing aqueous phytosphingosine solution
-
Solvent
system for enhancing solubility
-
Pharmaceutical composition comprising cyclosporin
-
Thickened aqueous surfactant solutions
-
Aqueous drink composition comprising ibuprofen
-
Stable
calcitriol solution for packaging into vials
-
Solution
containing nicotine
-
Aqueous
solution of t-PA
-
Stabilizing
solutions for proteins and peptides
-
Thickened
hydrolyte isotonic beverage
-
Cosolvent
formulations
-
Oxybutynin
formulations and method of use
-
Cyanamide
aqueous solution
-
Transparent
aqueous solution of diclofenac sodium and medicinal compositions with
the use of the same
-
Pharmaceutical
formulations of taxanes
-
Solubility
parameter based drug delivery system and method for altering drug
saturation concentration
-
Stable
aqueous solution having high concentrations of calcium and phosphate
ions and solid complex
-
Supersaturated
ascorbic acid solutions
-
Compositions
and method for treating migraine
-
Solubilisation
aids
Drug Delivery System, Sponge
-
Hemostatic sponge based on collagen
Drug Delivery System, Spray, Nasal/Dermal/Others
-
Nasal spray steroid formulation and method
-
Nasal spray for treating streptococcal infections
-
Topical spray for burn
treatment and anti-infection
-
Spray composition
-
Nasal spray compositions
-
Film forming compositions for topical use and
delivery of active ingredients
-
Sprayable analgesic composition and method of use
-
Nasal spray for decongesting nasal passages
-
Topical spray for burn treatment and
anti-infection
- Proanthocyanidins
and ascorbic acid composition for topical application to human
respiratory and oral mucosa
- Antihistamine sprays and ointments for relief of
delayed contact dermatitis
Drug Delivery System, Sublingual
-
Orodispersible
pharmaceutical composition for oromucosal or sublingual administration of
agomelatine
-
Human chorionic
gonadotropin (hCG) formulations for facilitating weight loss and body
contouring
-
Sublingual compositions comprising thymosin
fraction 5 and methods for administration thereof
-
Administration of dihydroergotamine as a
sublingual spray or aerosol for the treatment of migraine
-
Sublingual oral dosage form
-
Buccal
and sublingual administration of physostigmine
-
Sublingual
buccal effervescent
Drug Delivery System, Sunscreen/Tanning
-
Sunscreen safety
and efficacy enhancement
-
Therapeutic soap product
with UV protection
-
Topical acne vulgaris medication with a
sunscreen
-
Sulfur-modified zinc
oxide
-
Topical acne vulgairs medication with a sunscreen
-
Stabilized sunscreen composition having a particulate inorganic
sunscreen
-
Sunscreen composition
-
Sunscreen formulations containing nucleic acids
-
Sunscreen compositions
-
Composition containing a peptide and a pigment
and the use thereof in darkening the skin
-
Plant-based non-toxic sunscreen products
-
Sunscreen compositions
-
Tyrosinase inhibitors from plants
-
Sun-protection formulations active against herpes
simplex viruses
-
Enhanced SPF sunscreen (sprayable) formulations comprising
interpolymers of PVP/dimethiconylacrylate/polycarbamyl/polyglycol
ester
-
Method
for preparing ultraviolet radiation-absorbing compositions
-
Sunscreen
with disappearing color indicator
-
Delivery
system for inorganic sunscreens
-
Method,
apparatus, and composition for automatically coating the human body
-
Composition
for protecting skin from damaging effects of ultraviolet light
-
Ultraviolet-screening
zinc oxide excellent in transparency and composition containing the
same
-
Sunscreen
having disappearing color
-
Sunscreen
formulation with avobenzone and method for stabilizing sunscreen
formulation which contains avobenzone
-
Powder
coated with sparingly soluble ultraviolet absorber
-
Delivery
system for suncare products
-
Sunscreen
applicator system
-
High
SPF sunscreen formulations
-
High
efficiency skin protection formulation with sunscreen agents and
antioxidants
-
Substantive
topical composition
-
Use
of emu oil for stimulating skin and hair growth
-
Sunscreen
compositions
-
Sunscreen
cosmetic composition
Drug Delivery System,
Suppository/Rectal
-
Urogenital or anorectal,
transmucosal vaccine delivery system
-
Suppository of retaining in lower region of rectum
-
Percutaneously applicable preparation and
suppository containing an antidementia medicament
-
Suppositories
- Controlled,
phased-release suppository and its method of production
- Suppository
containing an antidementia medicament
- JM216
formulations
- Long-lasting
composition for rectal administration
- Vaginal
suppository vaccine for urogenital infections
- Pharmaceutical
suppository composites for fever and influenza and method of producing
the composites
- Unit
galenical formulation for local hormonotherapy of vaginal dryness
- Method
of the manufacture of suppositories
Drug Delivery System,
Supramolecular Complex
- Orally
deliverable supramolecular complex
Drug Delivery System, Surfactant
-
Surfactants that mimic the glycocalyx
-
Aqueous surfactant compositions of monoalkyl
phosphate ester salts and amphoteric surfactants
- C7
-C12 Diol & Diol alkoxylates as coupling agents for
surfactant formulations
Drug Delivery System, Suspension/Dispersion
-
Oral
pharmaceutical formulation in the form of aqueous suspension of
microcapsules for modified release of amoxicillin
-
Aqueous
suspension of nanoscale drug particles from supercritical fluid
processing
-
Pharmaceutical
compositions for bioactive peptide agents
-
Stabilized
dispersions comprising excipient surface-modified organic nanoparticles
and medicament particles
-
Oral pharmaceutical suspension of Cefdinir
crystal
-
Colloidal suspension of submicronic particles as vectors for active
principles and method for preparing same
-
Stabilized bioactive preparations and method of use
-
Thickener for
high-surfactant aqueous systems
-
Microprecipitation method for preparing submicron suspensions
-
Composition comprising ubiquinone
-
Polyol/oil suspensions for the sustained release of proteins
-
Method for preparing submicron suspensions with polymorph control
-
Stable non-dihydrate azithromycin oral
suspensions
-
Liquid dispersion polymer compositions, their
preparation and their use
-
Drinkable ibuprofen pharmaceutical suspension
-
Stable protein and nucleic acid formulations
using non-aqueous, anhydrous, aprotic, hydrophobic, non-polar vehicles
with low reactivity
-
Preparing aqueous polymer dispersions
-
Process for preparing an oral suspension of a
pharmaceutical substance
-
Stable particle in liquid formulations
-
Preparation of injectable suspensions having
improved injectability
-
Method for forming an aqueous flocculated
suspension
-
Microprecipitation method for preparing submicron
suspensions
-
Flocculated suspension of megestrol acetate
-
Process for preparing a crystal suspension
-
Excipient for the lyophilization of aqueous
suspensions of microparticles
-
Sonic method of enhancing chemical reactions to
provide uniform, non-agglomerated particles
-
Nonaqueous fluorinated drug delivery suspensions
-
Hydrocarbon gels as suspending and dispersing
agents and products
-
Suspension
of sparingly water-soluble acidic drug
-
Taste
masked liquid suspensions
-
Pharmaceutical
suspension comprising nevirapine hemihydrate
-
Stabilized
ascorbic acid, composition, and method of use
-
Fluidized
polymer suspensions of cationic polysaccharides in polyols and use
thereof in personal care compositions
-
Process
and composition for therapeutic cisplatin (CDDP)
-
Sterilization
process for pharmaceutical suspensions
-
DASC
compositions, process for preparing same and suspensions containing
same
-
Decongestant/antihistaminic
compositions
-
Ultra-fine
microcrystalline cellulose compositions and process
-
Flocculated
suspension of megestrol acetate
-
Fluid
suspension of polysaccharides for personal care and household
applications
-
Enhancement
of guar solution stability
Drug Delivery System,
Sweetener, Artificial
-
Method of improving sweetness delivery of sucralose
-
Anhydrous lactitol crystals, a product containing
the same and a process for the preparation thereof as well as use thereof
-
Method of improving sweetness delivery of sucralose
Drug Delivery System, Syrup
-
Stabilized antihistamine syrup
-
Stabilized antihistamine syrup
Drug Delivery System,
Tablet/Caplet/Compressed Dosage Form
-
Vaginal tablets
comprising misoprostol and methods of making and using the same
-
Direct
compressible trehalose solids
-
Solid dosage form of
wetted heparin
-
Tablet composition with a
prolonged release of tamsulosin
-
Pharmaceutical tablet
system that floats on gastric fluid for multipulse release of active
substance, and respective processes of producing same and a cup-shaped
envelope of same
-
Fast dissolving tablet
and method of preparing the same
-
System for delaying drug
delivery up to seven hours
-
Stable tablet
formulation
-
Pharmaceutical safety
dosage forms
-
Methods and apparatus
for determining formulation orientation of multi-layered pharmaceutical
dosage forms
-
Orally
disintegrable tablets
-
Modified release
oral dosage form using co-polymer of polyvinyl acetate
-
Tabletting process
-
Process for
producing solid dosage forms
-
Stable
pharmaceutical formulation of paroxetine hydrochloride anhydrous and a
process for preparation thereof
-
Ondansetron orally disintegrating tablets
-
Pharmaceutical
composition for compressed annular tablet with molded triturate tablet for
both intraoral and oral administration
-
Sustained
release formulations containing acetaminophen and tramadol
-
Modified calcium
phosphate excipient
-
Simethicone containing tablet composition
and method
-
Multilayer dosage forms containing NSAIDs
and triptans
-
Pharmaceutical tablets having height greater
than width
-
Directly compressible
tricalcium phosphate
-
Methods for targeted
drug delivery
-
Stable pharmaceutical compositions containing
7-substituted-3,5-dihydroxyheptanoic acids or
7-substituted-3,5-dihydroxyheptenoic acids
-
Stable pharmaceutical
formulation of paroxetine hydrochloride and a process for preparation
thereof
-
Process for producing an
oral sustained-release preparation of fasudil hydrochloride
-
Rapidly disintegrating methylcellulose tablets
-
Processes for the
preparation of oral dosage formulations of modafinil
-
Directly compressible formulations of azithromycin
-
Stabilized pharmaceutical and thyroid hormone compositions and
method of preparation
-
Controlled absorption diltiazem pharmaceutical formulation
-
Fast disintegrating tablet
-
Fenofibrate
pharmaceutical composition having high bioavailabilty
-
Soft chewable tablets
-
Method for preparing
solid dosage form of desmopressin
-
Second release phase formulation
-
Bitterness-reduced intrabuccally quick disintegrating tablets and method
for reducing bitterness
-
Process for the
preparation of directly compressible α-mannitol
-
Once a day antihistamine
and decongestant formulation
-
Bioadhesive tablet containing testosterone/testosterone ester mixtures and
method for producing a predetermined testosterone time-release profile
with same
-
Paroxetine controlled release compositions
-
Water soluble powders and tablets
-
Storage stable thyroxine active drug formulations and methods for their
production
-
Pharmaceutical excipient having improved compressibility
-
Chrono delivery formulations and method of use
thereof
-
Stable pharmaceutical compositions without a stabilizer
-
Directly compressible raw material for tablets
-
Once-a-day controlled release sulfonylurea
formulation
-
Dosage forms and methods for oral delivery of
progesterone
-
Process for preparing a directly compressible
solid dosage form containing microcrystalline cellulose
-
Pharmaceutical composition for compressed annular tablet with molded
triturate tablet for both intraoral and oral administration
-
Production of a directly compressible tabletting
aid
-
Microcrystalline cellulose cushioning granules
-
Stabilization of solid thyroid drug formulations
-
Directly compressible high load acetaminophen
formulations
-
Rapidly expanding starches with altered
crystalline structure
-
Amylose products as matrix former for programmed
release systems, process for preparing these amylose products, and process
for making programmed release systems
-
Powdered/microfibrillated cellulose
-
Technical field
(quick disintegrating tablet)
-
Substituted benzimidazole dosage forms and method
of using same
-
Process for the preparation of direct tabletting
formulations and aids
-
Amoxicillin and potassium clavulanate dosage form
-
Process for preparing non-hygroscopic sodium
valproate composition
-
Modified release pharmaceutical formulation
comprising amoxycillin
-
Pharmaceutical excipient having improved
compressibility
-
Fast dissolving tablet
-
Orodispersible tablets containing fexofenadine
-
Method for increasing the active loading of
compressible composition forms
-
Use of an acrylic type polymer as disintegrating
agent
-
Exactly divisible tablet
-
Filler binder for tablets
-
Aqueous dispersion suitable for the production of
coatings and binders for solid oral drugs
-
Fenofibrate pharmaceutical composition having high bioavailability
-
Instant granules and process for their
formulation
-
Bioadhesive progressive hydration tablets
-
Dispersible and soluble galenic paracetamol
formulation, method for its preparation and its applications
-
Solid dose forms containing bismuth
-
Oral pulsed dose drug delivery system
-
Dispersible macrolide compounds and method for production thereof
-
Highly compressible ethylcellulose for tableting
-
Simple tablet compression using gelatin
-
Pharmaceutical excipient having improved
compressibility
-
Compressed nitroglycerin tablet and its method of
manufacture
-
Binder-free compacted forms of
1,3-dihalo-5,5-dimethylhydantoins
-
Tablet shapes to enhance gastric retention of
swellable controlled-release oral dosage forms
-
Process for manufacturing bite-dispersion tablets
-
Pharmaceutical excipient having improved
compressibility
-
Chargeable
pharmaceutical tablets
-
Gellan gum tablet coating
-
Directly
compressible high load acetaminophen formulations
-
Use
of lipids as adjuvents in the production of solid medicinal forms by
the melt extrusion process
-
Self-destructing,
controlled release peroral drug delivery system
-
Pharmaceutical excipient having improved
compressibility
-
Dividable
tablet and press-through pack
-
Abuse
resistant tablets
-
Quickly
disintegratable compression-molded materials and process for producing
the same
-
Apparatus
and method for tablet fabrication
-
Pulverulent
sorbitol and its process of preparation
-
Directly
compressible, ultra fine acetaminophen compositions and process for
producing same
-
Bioadhesive
progressive hydration tablets and methods of making and using the same
-
Sustained
release matrix for high-dose insoluble drugs
-
Dissolution
of triprolidine hydrochloride
-
Directly
compressible high load acetaminophen formulations
-
Pharmaceutical
excipient having improved compressibility
-
Solid,
non-deliquescent formulations of sodium valproate
-
Impeding
the extraction of active ingredients out of tablets
-
Tablet
dosage form of clavulanic acid and amoxycillin comprising a trehalose
excipient
-
Stabilized
thyroxine medications
-
Solid
pharmaceutical composition comprising an excipient capable of binding
water
-
Stabilized
pharmaceutical composition of a nonsteroidal anti-inflammatory agent
and a prostaglandin
-
Once
daily analgesic tablet
-
Pharmaceutical
tablet designed for easier breaking
-
Low-dosed
steroid tablets that contain gallic acid ester as an antioxidant,
process for production, and use
-
Healthful
dissolvable oral tablets, and mini-bars
-
Free-flowable
directly compressible starch as binder, disintegrant and filler for
compression tablets and hard gelatine capsules
-
Tablet
containing a coated core
-
Pharmaceutical
matrix pellets, tablets and composition for the preparation thereof
-
Oral
pharmaceutical dosage forms comprising a proton pump inhibitor and a
prokinetic agent
-
Controlled-release,
drug-delivery tableted composition including a complex between
poly(maleic diacid-alkyl vinyl ether) and polyvinylpyrrolidone
-
Stable
compositions containing N-propargyl-1-aminoindan
-
Cisapride
sustained release
-
Direct
compression metformin hydrochloride tablets
-
Solid
compositions containing polyethylene oxide and an active ingredient
-
Paroxetine
tablets and process to prepare them
-
Cisapride
mini-tablet formulations
-
Multiparticulate
tablet disintegrating in less than 40 seconds in the mouth
-
Once
daily analgesic tablet
-
Pharmaceutical
excipient having improved compressibility
-
Dry
mix formulation for bisphosphonic acids
-
Tablet
containing an enzymatically converted starch derivative encapsulating
agent
-
Layered
tablet for the controlled release of active substances
-
Direct
compression carbonyl iron tablet
-
Controlled
release tablet compositions
-
Cholesterol-lowering
tablets
-
Use
of redispersible polymer powders or polymer granules as binders for
producing solid pharmaceutical presentations
-
Compressed
dry-granulation desogestrel tablets
-
Bioadhesive
tablet
-
Rapid-release
S1452 tablets
-
Preblend
of microcrystalline cellulose and lactase for making tablets
-
Orally
administrable solid dosage form
-
Polymer
coated tablet comprising amoxycillin and clavulanate
-
Fast-dissolving
comestible units formed under high-speed/high-pressure condition
-
Decongestant/antihistaminic
compositions
-
Method
and apparatus for preparation of molded tablet and thereby prepared
molded tablet
-
Rapid
release tablet comprising tolfenamic acid or a pharmaceutically
acceptable salt thereof
-
Controlled
release tablet of bupropion hydrochloride
-
Potassium,
sodium and tris oxaprozin salt pharmaceutical formulations
-
Process
and apparatus for the production of divisible tablets
-
Starch
products as tabletting excipient, method for preparing same, and
method for making tablets
-
Pharmaceutical
compositions containing irbesartan
-
Cross-linked
cellulose as a tablet excipient
-
Self-binding
shearform compositions
-
Directly
compressible high load acetaminophen formulations
-
Pharmaceutical
suspension tablet compositions
-
Pharmaceutical
formulations having improved disintegration and/or absorptivity
-
Oral
pharmaceutical composition with delayed release of active ingredient
for pantoprazole
-
Controlled
release tablet
-
Local
oral herbal slow release tablets
-
Method
for making fast-melt tablets
Drug Delivery System, Tamper
Resistant
-
Abuse-deterrent
pharmaceutical compositions of opiods and other drugs
-
Pharmaceutical formulation containing opioid
agonist, opioid antagonist and irritant
-
Material for controlling
diversion of medications
-
Tamper-resistant oral opioid agonist formulations
Drug Delivery System,
Targeted/Cell-Specific
-
Cardiac targeted
delivery of cells
-
Targeting of
glycoprotein therapeutics
-
Targeted
therapeutic agent release devices and methods of making and using the
same
-
Targeted
drug-carrying bacteriophages
-
Drug delivery to a
joint
-
Gene delivery vectors
provided with a tissue tropism for smooth muscle cells, and/or endothelial
cells
-
Buoyant polymer
particles for delivery of therapeutic agents to the central nervous system
-
Membrane active
polymers
-
Immunoliposomes
that optimize internationalization into target cells
-
Transporter
protein
-
Method for in vivo
delivery of active compounds using reagent conjugate
-
Method for
treatment directed to agent retention in biological tissues
-
Selective targeting of
apoptotic cells
-
Methods for
delivering compounds into a cell
-
Methods for
producing target cell reactive lymphocytes
-
Delivery carrier for
targeting to cells expressed with somatostatin receptors
-
Cell
penetrating peptides for intracellular delivery of molecules
-
Compositions
and methods for intracellular delivery of biotinylated cargo
-
Method for
delivering a biological compound using neural progenitor cells derived
from whole bone marrow
-
Compounds for
targeting hepatocytes
-
Compositions and methods for identifying and targeting cancer cells of
alimentary canal origin
-
Tissue specific
prodrugs
-
Compositions and
methods of use of targeting peptides against placenta and adipose tissues
-
Use of
nanoparticles for the DNA administration to a target organ
-
Subcellular
targeting of therapeutic proteins
-
Pharmaceutical
and diagnostic compositions containing nanoparticles useful for treating
targeted tissues and cells
-
Induction of a
protective immune response through microprojectiles coated with a DNA
sequence encoding an immunogenic protein
-
Labile linkage for compound delivery to a
cell
-
Transferring materials into cells using
porous silicon
-
Device and methods for sequential, regional
delivery of multiple cytotoxic agents and directed assembly of wound
repair tissues
-
Materials and methods relating to polyions
and substance delivery
-
Multidrug multiligand conjugates for targeted drug delivery
-
Methods and compositions
for directing cells to target organs
-
Targeting drug/gene carriers to irradiated tissue
-
Anti-MUC-1 single chain antibodies for tumor targeting
-
Nuclear targeting by
means of bacterial proteins
-
Enhancement of intracellular delivery and tissue targeting of drugs and
genes
-
Technology of
intracellular delivery of DNA oligonucleotides to improve drug activity
-
Systems and methods for delivering drugs to selected locations
within the body
-
Targeted cytolysis of HIV-infected cells by chimeric CD4 receptor-bearing
cells
-
Method to provide bacterial ghosts provided with antigens
-
X-ray guided drug delivery
-
Process for generating multilayered particles
-
Intracellular delivery of biological effectors
-
Drug targeting system, method of its preparation and its
use
-
Methods for introducing mannose 6-phosphate and other
oligosaccharides onto glycoproteins
-
Cellular delivery agent
-
Temperature sensitive control of liposome-cell adhesion
-
Compositions and methods for tumor-targeted delivery of effector molecules
-
Intracellular delivery of biological effectors
-
Microprojectile delivery system and particulate product
-
Peyer's patch and/or M-cell targeting ligands
-
Targeted delivery via biodegradable polymers
-
Methods for identifying and isolating tissue-specific lumen-exposed
molecules
-
Identification of peptides that facilitate uptake
and cytoplasmic and/or nuclear transport of proteins, DNA and virues
-
Chimeric proteins for use in transport of a
selected substance into cells
-
Enhanced transport using membrane disruptive
agents
-
Methods for rapidly identifying small organic
molecule ligands for binding to biological target molecules
-
VZV ORF29p protein-related compositions and
methods
-
Polyampholytes for delivering polyions to a cell
-
Human monoclonal antibody specifically binding to
surface antigen of cancer cell membrane
-
Sequence and method for genetic engineering of
proteins with cell membrane translocating activity
-
Method for targeted delivery of nucleic acids
-
Transition metal complexes of n,
n',n"trialkyl-cis-1,3,5-triaminocyclohexane and related compositions and
methods of synthesis and use
-
Targeted liposome gene delivery
-
Viral recombinant vectors for expression in
muscle cellsv
-
Antibody/receptor targeting moiety for enhanced
delivery of armed ligand
-
Drug delivery formulations and targeting
-
Method of targeting pharmaceuticals to motor
neurons
-
Tissue-vectors specific replication and gene
expression
-
Targeted vectors
-
Agents to increase the uptake of pharmaceuticals
and diagnostic substances into solid tumors
-
Amino acid substitution mutants of interleukin 13
-
Materials and methods for intracellular delivery
of biologically active molecules
-
Molecules that home to various selected organs or
tissues
-
Cellular targeting poly(ethylene glycol)-grafted
polymeric gene carrier
-
Ion exchange tumor targeting (IETT)
-
Fibrin nanoparticles and uses thereof
-
Cell membrane-directed drugs
-
High efficiency tissue specific compound delivery system using
streptavidin-protein a fusion protein
-
Method for importing biologically active
molecules into cells
-
Hybrid compositions for intracellular targeting
-
Pharmaceuticals and assays using enzyme subunits
-
Covalent microparticle-drug conjugates for
biological targeting
-
Methods and compositions for delivery of
therapeutic agents to bone tissue employing conjugates of negatively
charged peptide oligomers with therapeutic agents
-
Genetically modified tumor-targeted bacteria with
reduced virulence
-
Covalent polar lipid conjugates with
neurologically active compounds for targeting
-
Non-invasive
gene targeting to the brain
-
Methods
and compositions for increasing the target-specific toxicity of a
chemotherapy drug
-
Tumor
specific internalizing antigens and methods for targeting therapeutic
agents
-
Conjugate
of biologically active compound and polar lipid conjugated to a
microparticle for biological targeting
-
Method
of intracellular binding target molecules
-
Tat-derived transport polypeptides
-
Method
of identifying molecules that home to a selected organ in vivo
-
Heart
homing peptides and methods of using same
-
Localization
and therapy of non-prostatic endocrine cancer with agents directed
against prostate specific antigen
-
Delivery
of biologically active substance to target sites in the body of
patients
-
Conjugates
targeted to the interleukin-2 receptor
-
Molecules
that home to various selected organs or tissues
-
Cell-specific
contrast agent and gene delivery vehicles
-
Osmotic
delivery composition, solution, and method
-
Immunoliposomes
that optimize internalization into target cells
-
Materials
and methods for intracellular delivery of biologically active
molecules
-
Materials
and methods for the intracellular delivery of substances
-
Lipid-modified
insulin incorporated liposomes for selectively delivering cytotoxic
agents to hepatoma cells
-
Targeted
polymerized liposome diagnostic and treatment agents
-
Cell-specific
molecule and method for importing DNA into a nucleus
-
Drug
targeting to the nervous system by nanoparticles
-
In
vivo agents comprising cationic drugs, peptides and metal chelators
with acidic saccharides and glycosaminoglycans, giving improved
site-selective localization, uptake mechanism, sensitivity and
kinetic-spatial profiles, including tumor sites
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Receptor
ligand-facilitated delivery of biologically active molecules
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Site-directed
chemotherapy of metastases
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Colonic
delivery of protein or peptide compositions
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DNA
molecule encoding for cellular uptake of Mycobacterium tuberculosis
and uses thereof
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Method
of identifying molecules that home to a selected organ in vivo
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Localization
and therapy of non-prostatic endocrine cancer with agents directed
against prostate specific antigen
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Targeted
delivery of genes encoding interferon
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Drug
delivery using terminal complement components
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Colon
targeted delivery system
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Compositions
containing nucleic acids and ligands for therapeutic treatment
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Targeted
delivery of poly- or oligonucleotides to cells
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Covalent
polar lipid conjugates with neurologically active compounds for
targeting
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Targeted forms of methyltrithio antitumor agents
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Delivery
of diagnostic and therapeutic agents to a target site
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Method
for delivering bioactive agents into and through the mucosally-associated
lymphoid tissues and controlling their release
Drug Delivery System, Taste Masking/Mouthfeel
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Taste-masked
composition of cationic exchange resin
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Fast dissolving orally
consumable films containing a taste masking agent
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Film-shaped or
wafer-shaped pharmaceutical preparation with masked taste
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Liquid drug
preparations
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Inhibitors of
the bitter taste response
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Controlled release and
taste masking oral pharmaceutical compositions
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Controlled release and
taste masking oral pharmaceutical composition
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Human T2R61 taste
receptor and related assays for identifying human bitter taste modulators
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Taste masked veterinary formulation
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Coating compositions for
bitterness inhibition
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Pharmaceutical
formulation having a masked taste and method for the production thereof
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Particle formation
methods and their products
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Ibuprofen composition
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Bitterness-reduced intrabuccally quick disintegrating tablets and method
for reducing bitterness
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Particles coated with granulated crystalline ibuprofen
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Nucleotide compounds that block the bitter taste of oral compositions
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Liquid pharmaceutical composition
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Taste masked liquid pharmaceutical compositions
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Taste masked pharmaceutical compositions
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Taste masking rapid release coating system
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Bitterness-reduced oral pharmaceutical
composition
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Orally administrable compositions comprising
cation cross-linked polysaccharide and a polymer digestible in the lower
gastrointestinal tract
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Masking agent in powder form for pharmaceutical
tastes
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Pediatric formulation of gatifloxacin
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Medicinal compositions with relieved bitterness
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Taste masking coating composition
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Inhibitors of the bitter taste response
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Taste masking of oral quinolone liquid preparations using ion exchange
resins
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Pulverulent
sorbitol and its process of preparation
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Taste-masked pharmaceutical composition
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Taste
modified hard confectionery compositions containing functional
ingredients
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Tablets
containing a sweetening mixture
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Rapidly
releasing and taste-masking pharmaceutical dosage form
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Granular
preparation and producing process thereof
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Taste
masked liquid suspensions
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Flavor
blend for masking unpleasant taste of zinc compounds
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Dosage
forms containing taste masked active agents
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Method
and composition for masking mineral taste
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Taste-masked
formulations
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Taste
of active pharmaceutical ingredients
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Flavor-masked
pharmaceutical compositions
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Oral
compositions having enhanced mouthfeel
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Croscarmellose
taste masking
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Taste
masking pharmaceutical composition for oral administration
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Taste
masking of phenolics using citrus flavors
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Taste
masked desensitizing compositions
Drug Delivery System,
Teorell-Meyer Gradient
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Drug dosage form based on the teorell-meyer gradient
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