1-NEP N-һͪ
1-NMP N-ͪ
2G--CYD ǻ
2-HP--CYD 2DZ
5-NCP 5-Ȼͪ
5-NMP 5-ͪ
Accelerated testing
Acrylic acid resin ϩ
Active targeting preparation Ƽ
Adersive dispersion-type TTS ճɢTTS
Adhersive strength ճ
Adhesion ճ
Adhesives ճϼ
Aerosil ۹轺
Aerosol
Aerosol of micropowders for inspiration
Aethylis oleas
Agglomerate ۽
Aggregation ۼ
Air suspension
Alarm clock
Alcohol Ҵ
All-trans ȫʽ
Alterntae addition method ཻ뷨
Amebocyte lysate ϸܽ
Amorphous forms
Angle of repose ֹ
Antiadherent ճ
Antioxidants
Antisepesis
Apparent solubility ܽ
Aprotinin ̪ø
Aquacoat һάˮɢ
Aromatic waters ˮ
Arrhenius ˹
Ascabin ᡡ
Aseptic technique
Azone ͪ
Azone ͪ
Ball mill ĥ
Base adsorption
Bases
Beeswax
Bending
BHA 嶡ǻ
BHT 嶡Լ
Bioavailability ö
Biochemical approach ѧ
***aceutics ҩѧ
Biotechnology \
Bondѧ˵ еȷ飨
Bound water ˮ
Breakage (Bk)
Brij ϩ֬
Brij ϩ֬
Buccal tablets նƬ
Bulk density ܶ
Bulk density ܶȡܶ
Burst effect ͻЧӦ
CA ά
CAB άض
Cabomer ǻϩ
Caking
CAP ά̪
CAP ڱά
CAP ڱά
CAP ڱά
CAP ڱά
Capillary state ëϸ״
Capsules Ҽ
Carbomer ķȻϩ
Carbopol
Carbopol 934
Carboxymethyl cellulose sodium Ǽά
Carboxymethyl starch sodium CMS-Naȼ
Carboxymethylcellulose sodium CMC-Naȼά
CAT άر
CD Բɫ
Cellulose acetate (CA) ά
Cellulose acetate phthalate (CAP) ά̪
Central composite design (CCD) ǵ
Cera aseptical pro osse bone wax
Ceramide
Cetomacrogol Ҷʮ
Chemical approach ѧ
Chewable tablets Ƭ
Chitin Ƕ
Chitosan Ǿ
Chronopathology ʱѧ
Chronopharmacology ʱҩѧ
Clausius-Clapeyron ˹
Clinical pharmaceutics ٴҩѧ
Cloud point ԾϩͷӱԼ
CMC-Na ȼά
CMC-Na ȼά
CMC-Na Ǽά
CMEC ȼά
CMS ȼ
CMS-Na ȼ
Coadminiatration of skin Meta Inh ƤлƼĺ
Coadministraition of chem. P Enh ѧմٽĺ
Coagulation ۳
Coated tablets Ƭ
Coating material
Cocoa butter ɿɶ֬
Cohesion ԡճ
Cohesive strength ھ
Cold compression method ѹ
Cold-homogenization ȴһȻ
Colon-targeted capsules ᳦Ҽ
Compactibility
Complex coacervation ۷
Compliance ˳Ӧ
Compliance ˳Ӧ
Compressed tablets ͨƬ
Compressibility ѹ
Compressibility ѹ
Compression ѹ
Compressive work ѹ
Cone and plate viscometer Բƽճȼ
Consistency curve
Controllability ɿ
Controlled release tablets Ƭ
Controlled-release preparation Ƽ
Convective mixing
Convective transport
Coordination number λ
Copoly (latic/glycolic) acid ҴṲ
Core material
Cosolvency DZ
Cosolvency DZ
Cosolvent DZܼ
Cosolvent DZܼ
Coulter counter method ؼ
Count basis
CP ϩ
CPVP ϩȿͪ
CRacemization
Creams
Creep
Cremolphore EL ϩ
Critical relative humidity (CRH) ٽʪ
Critical relative humidityCRH ٽʪ
Critical velocity ٽٶ
Critrical micell concentration CMCٽ罺Ũ
Croscarmellose sodium CCNaȼά
Croscarmellose sodium (CCNa) ά
Crospovidone άͪ
Cross-liked polyvinyl pyrrolidone PVPPάͪ
Crushing
Crystal form
Crystal habit ̬ᾧϰ
CTS ͨ˨
Cumulative size distribution ۻֲ
Cutting
Cyclodextrin (CYD)
Cylinder model Բ˨ģ
Cytotoxicity ϸ
DDS ҩﴫϵͳ
Decoction
Degree of circularity Բζ
Degree of sphericility ζ
Delipidization ʲȥ֬ʻ
Dextrin
Dialysis cell method ط
Dicetyl phosphate ֬
Dielectric constant 糣
Differential scanning calorimetry DSCʾɨȷ
Differential thermal analysis DTAʾȷ
Diffusive mixing ɢ
Dilatant flow
Diluents ϡͼ
Dimethicone (silicones) ͪ͡͡
Dimethyl sulfoxide(DMSO)
Dimethylacetamide (DMA)
Disinfection
Disintegrants
Disk assemble method Բ̷
Disperse medium ɢ
Disperse phase ɢ
Disperse system ɢϵ
Dispersed phase ɢࡢࡢ
Dispersible tablets ɢƬ
Displacement value (DV) û
Distilled water ˮ
DL-phenylalanine ethyl acetoacetate DL
DLVO
DME
DMSO Ƿ
DM--CYD
Donor cell
DOPE ֬Ҵ
DOPE ֬Ҵ
Dosage form ҩ
DPPC ֬
DPPC ֬
Drop dentifrices
Drug carrier ҩ
Drug-loading rate ҩ
Dry bulb temperature ¶
DSPC Ӳ֬֬
DSPE Ӳ֬֬Ҵ
Dumping effect ͻЧӦ
EA һά
Ear drops ζ
EC һά
EC ëϸܵӾ
EC һά
EC һά
EC һά
EC һά
Effect diameter Dsk,Ч
Effectiveness Ч
Effervescent disintegrants ڱ
Effervescent tablets Ƭ
Elastic deformation Ա
Elastic recovery (ER) Ըԭ
Elastic work Թ
Elasticity
Electro phoresis Ӿ
Electroporesis ¿
Electuary
EMA ױϩ
Emolphor ϩͻ
Emulsifer in water method ˮ黯ʪ
Emulsifier in oil method 黯ɽ
Emulsion ͨ
Emulsions
Enamine ϩ
Endocytosis څ
Endotoxin ڶ
Enteric capsules ܽҼ
Enteric coated tablets Ƭ
Entrapment rate
Epidermis Ƥ
Epimerization 칹
EPRЧӦ
Equilibrium solubility ƽܽ
Equilibrium water ƽˮ
Equivalent specific surface DSV
Equivalent volume diameter Dvȼ۾൱
Ethanol Ҵ
Ethical (prescription) drug ҩ
Ethycellulose (EC) һά
Ethylcellulose ECһά
Ethylene vilnylacetate copolymer ϩ-ϩ
Ethylene vinylacetate copolymer ϩϩ
Eu L, Eu S ۼϩ
Eu RL, Eu RS ۼϩ
Eu RL100, Eu RS100 ϩܣ
Eu RL100, Eu SL100 ۱ϩ֬ϵ
Eu S100, Eu L100 ϩṲܣ
Eudragit (E, RL, RS) ϩ
Eudragit L100 ϩṲ
Eudragit RS100, RL100, NE30D ϩṲ-
Eudragit S100 ϩṲ
EVA ϩϩ
EVA ϩϩ
EVA ϩ-ϩ
EVA ϩ-ϩ
Evaporation
Excipients (adjuvants)
External phase ɢʡࡢ
Extracts
Eye drop ۼ
Eye ointments ۸
Factorial design
Fatty oils ֬
Feret diameter ߾
Ficksһɢʽ ҩȡ
Fillers
Film coated tablets ĤƬ
Film dispersion method ɢ
Films Ĥ
First-pass effect ЧӦ
Fliud extracts
Flocculation
Flocculation
Flocculation value
Flow curve
Flow velocity ٶ
Flowability
Fluid-energy mills ĥʽ
Fluidity buffer Ի
Fluidized bed coating ·
Free water ˮ
Freely movable liquid Һ
Freon ࡢﰺ
Frequency size distribution Ƶʷֲ
Funicular state ״
Fusion ں
Fusion method ӷ
Garles
GAS 巴ܼ
Gas adsorption method
Gas antisolution GAS
Gas permeability method
GCP ҩٴ淶
Gelatin ֽ
Gelatin
Gelatin glycerin ֽ
Gelatinization
General acid-base catalysis
Geometric diameter ѧӾ
Geometric isomerization 칹
Ghost cell Ӱϸ
Glidants
GLP ҩٴо淶
Glycerin
Glycerins ͼ
Glyceryl monostearate Ӳ֬ᡢ
Glycolic acid ǻ
GMP ҩƷ淶
Granule density ܶ
Granules
Graton-Fraserģ ģ
Group number HLB
Guest molecules ͷ
G--CYD ǣ
Half life ˥
Handerson-Hasselbachʽ ״̬pkcphĹϵ
Hard capsules ӲҼ
Hardness Ӳ
HCO DZ
HEC һά
HEMA ϩ
HES һ
Heywood diameter DhͶӰԲ൱
Higuchi ϣ
Host molecules
HPC DZά
HPC DZά
HPMA DZױϩ
HPMC DZά
HPMC DZά
HPMC DZά
HPMC DZά
HPMC DZά
HPMCAS DZά
HPMCAS DZά
HPMCAS DZά
HPMCP DZά̪
HPMCP DZάء
HPMCP Ǽά̪
HPMCP (HP-50, HP-55) DZά
Humidity ʪ
Hydration of stratum corneum ʲˮ
Hydrogel ˮ
Hydrophile-lipophile balance ˮƽֵ
Hydrotropy
Hydrotropy agent ܼ
Hydroxypropyl methylcellulose DZά
Hydroxypropyl methylcellulose acetate succinate DZά
Hydroxypropyl methylcellulose phthalate DZά̪
Hydroxypropylcellulose (HPC) DZά
Hydroxypropylcellulose (HPC) DZά
Hydroxypropylmethyl cellulose HPMCDZά
Hygroscopicity ʪ
Hypodermic tablets ƤעƬ
ICH Э
ICH Э
IDDS ֲҩϵͳ
IEC ӽɫ
IEF ȵ۽
Immobile liquid Һ
Impact
Impact mill ʽ
Implant tablets ֲƬ
Inclusion compound
Industrial pharmaceutics ҵҩѧ
Infusion solution Һ
Injection עҺ
In-liquid drying Һи黯ܼӷ
Interface polycondensation ۷
intra-arterial route ע
Intradermal (ID) route Ƥע
Intramuscular (IM) route ע
Intravenous (IV) route ע
Intrinsic dissolution rate ܳ
Intrinsic solubility ܽ
Inverse targeting
Iontophoresis
IR
Isoclectric focusing IEFȵ۽
Isoosmotic solution Һ
Isopropylpalmitate
Isostearylisostearate Ӳ֬Ӳ
Isotonic solution Һ
Isotonic solution Һ
Journal of Drug Targeting ҩ־
Kickѧ˵ ַ飨
Krafft point ͱԼ
Krummbein diameter
Lactic acid
Lactose
Lag time ʱ
Large unilamellar vesicles ֬
Laurocapam ¹ͪ
Length basis Ȼ
L-HPC ȡDZά
L-HPC ȡDZά
Limulus lysate test 鷨
Liniments
Liposomes ֬
Liquid immersion method Һ
Liquid injection Һע
Liquid paraffin Һʯ
Liquid paraffin ҺʯF
Long-circulating liposome ѭ֬
Long-circulating liposomes ѭ֬
Long-term testing
Loo-Rigelman ˫ѪҩŨȣʻ
Lotions ϴ
Lubricants
Lubricants
LUVs ֬
Martin diameter ȷ־
Mass basis
Matrix type Ǽ
Matrix-diffusion type TTS θɢTTS
Maximum additive concentration MACŨ
MC ά
MC ά
MC ά
MCC ά
Mechanical interlocking bonds ӼеǶ
Medicinal liquor Ƽ
Melt-homogenization ڣȻ
Membrane wall Ĥڿ
Membrane-moderated type TTS ĤTTS
Methyl acrylate-methacrylate co ϩ-ϩ
Methylcellulose (MC) ά
Methylcellulose (MC) ά
Micellar emulsion
Micelle
Microcapsules
Microcrystalline cellulose (MCC) ά
Microcrystalline cellulose (MCC) ά
Microemulsion
Microemulsion
Microencapsulation Ͱ
Micromeritics ѧ
Microreservoir-type TTS
Microscropic method
Microspheres
microstreaming
Minitablet СƬ
Mixing
Mixtures ϼ
MLVs ֬
MMA ϩ
Moistening agent ʪ
Moisture absorption ʪ
Molecular capsules
Multilamellar vesicles ౦֬
Multilayer tablets Ƭ
Multiorfice-centrifugal process ķ
Myrij ϩ֬
Myrj ϩ֬
Nacent soap method
Nanocapsule
Nanocapsules
Nanoemulsion
Nanoemulsion
Nanoliposomes ֬
Nanoparticles
Nanosphere
Nanospheres
Naonparticle
Nasal drops αǼ
Newtonian equation ţճȶ
Newtonian fluid ţ
Niosomes ֬壬
Nonbound water ǽˮ
Nonionic surfactant vesicles ӱԼ
Non-newtonian flow ţ
Non-Newtonian fluid ţ
Nonprescription drug Ǵҩ
Noyes-Whitney ܳٶȷ
NP -ͪ
Nucleation theory ɺ
OCDDS ڷ᳦λҩϵͳ
OCDDS ڷʱ(ʱ)ҩϵͳ
Ointments
Opitical isomerization ѧ칹
ORD ɫɢ
Orthologonal design
Osmotic pressure ѹ
OSSDDS ڷλҩϵͳ
Ostwald freundlich ᾧ
Over the counter (OTC) Ǵҩ
Oversize distribution ɸϷֲ
PA ֬
PACA ϩ
Packing fraction
Paints Ϳ
Paints ͿĤ
Pan coating ·
Paraffin ʯ
Particle size distribution ȷֲ
Partition coefficient (P) ϵ
Passive targeting preparation Ƽ
Patch
PB ۶ϩ
PBCA ϩᶡ
PCS ɢ❪
PE ϩ
PE ϩ
Peel tack test תʵ
PEG Ҷ
PEG Ҷ
PEG Ҷ
PEG-EG PEGε֬Ҵ
Pendular state Ӱ״
Penetration enhancers Ƥմٽ
PEO ϩ
PEO ϩ
PEO ϩ
Peregol O ϩ15ʹ
Perogol O ϩ15ʹ
PET ۶ԱҶ
PG
PGA Ҵ
Pharmaceutical engineering Ƽѧ
Pharmaceutical manufacturing Ƽ
Pharmaceutical preparation ҩƼ
Pharmaceutics ҩѧ
Pharmacia
Pharmacokinetics ҩﶯѧ
Pharmacological availability ҩö
Pharmacopoeia ҩ
Phase inversion critical point תٽ
Phase separation 뷨ѧ
Phase transition temperature תʪ
Phase volume ratio
Phonophoresis
Photodegradation ⻯
PHPMA DZױϩ
Physical and chemical T P ѧƼ
Physical approach ѧ
Physical pharmaceutics ҩѧ
PIB 춡ϩѹ
PiBCA ϩ춡
PiBCA ϩ춡֬
PLA
PLA
PLA
PLA/PGA, PLGA ҽ
PLA-PEG ҶǶι
Plastic deformation Ա
Plastic viscosity ճ
Plastisity
PLGA ҴṲ
PLGA ҽ
PLGA ҴṲ
PMMA ۼϩ
Poiseuile ʽ ʱҺ
Poloxamer (plurnic) ϩϩ
Poloxamer 188 (plurnic F68) ɳķ188F68
Poloxamer 188 (pluronic F68) ɳķ
Poloxamer 188 (Pluronic F68) ɳķ188F68
Poly (lactide-co-glycolide) ۱-ҽ
POLYACRYLICRESIN ۱ϩ
Polyalkylcyano-acrylate ϩ
Polydiethylene terephthalate ۶ԱҶ
Polyethylene ϩ
Polyethylene (PEG) Ҷ
Polyethylene glycol PEGҶ
Polyethylene glycol Ҷ
Polyethylene glycol (PEG) Ҷ
Polyethylene glycol (PEG) Ҷ
Polyethyleneglycol (PEG) Ҷ
Polymerization ۺ
Polymers in pharmaceutics ҩø߷Ӳѧ
Polymethyl methacrylate ۼϩ
Polymorphism ྦྷ
Polymorphism ྦྷ
Polyoxyethylene ϩ
Polyoxyl 40 stearate (Myri52) S-40ϩ40Ӳ֬
Polypropylene ۱ϩ
Polysorbate ɽ
Polyvinyl alcohol ϩ
Polyvinyl alcohol (PVA) ϩ
Polyvinyl chloride ϩ
Polyvinylpyrrolidine PVPάͪ
Polyvinylpyrrolidone άͪ
Porosity ϶
Porosity ϶
Povidone ϩȿͪ
Powder injection δע
Powders ɢ
PP ۱ϩ
PP ۱ϩ
Preformulation ǰ
Pregelatinized starch ۡԤۡѹԵ
Preservative
Pressure sensitive adhersive ѹ
Pressure-sensitive tape council ʵ
Prickle cell layer
Primary particle һ
Prodrug ǰҩ
propellents
Propylene glycol
Propylene glycol (PG)
PS(phosphatidylserine) ֬˿
PSA ѹ
Pseudo steady state α̬
Pseudoplastic flow
PSTC ʵ
Pulsed/pulsatile release ҩ
PVA ϩ
PVA ҽ
PVAP ϩ
PVC ϩ
PVC ϩ
PVC ϩ
PVP άͪ
PVP άͪ
PVP άͪ
PVP (PVPk15, PVPk30, PVPk90) άͪ
PVPP ϩȿͪ
PVPPPVP άͪ
Pycnometer ƿ
Pyrogen ԭ
QOL
Quasi-viscous flow ճ
Racemization
Raman
Random floc
Raoult ڶ
rapid expansion of supercritical S RESS
Rate of shear ٶȡʡٶݶ
Receptor cell ձ
Relative humidity RHʪ
Relative humidity (RH) ʪ
Response surface methodology ЧӦŻ
RESS ٽҺͼ
Retardants ͼ
Reverse osmosis
Rheology ѧ
Rittingerѧ˵ ϸ飨
Rolling ball tack test
RP-HPLC ЧҺɫ
Rubbing ĥ
Rumpf ʪ
SA Ӳ֬
Safety ȫ
Safflower غ컨
SDB-L-400 ۱ϩ
SDS, SLS ʮ
SDS-PAGE SDC۱ϩ
SEC ɫ
Second particle
SEDDSs 黯ҩﴫϵͳ
Sedimentation method
Sedimentation rate ݻ
Self-adjusted system Եʽҩϵͳ
SEM ɨ羵
Sensitization
Settling velocity diameter Ч
SFDA SFDA
Shape factor ״ϵ
Shear mixing л
Shearing force Ӧ
Sieving diameter Daɸ־
Sieving method ɸַ
Sieving method ɸַ
Simple coacervation ۷
Simplex method Ż
Single unilamellar vesicles С֬
Sink condition ©
Sink condition ©״̬
Size exclusion chromatography SEC
Slurry state ཬ̭
Sodium carboxymethyl starch Ǽ
Sodium lauryl sulfate (SDS) ʮջ
Sodium taurodihydrofusidate ţ˫ù
Soft capsules Ҽ
Soft paraffin ʯ
Solid bridges Ӽ
Solid lipid nanospheres (SLN) ֬
Solubility ܽ
Solubility parameter ܽȲ
Solubilization
Solubilization
Solubilization
Solubilizer ܼ
Solubilizer ܼ
Solution tablets ҺƬ
Solutions Һ
Solvent-nonsolvent ܼܼ
SOP
Soybean-derived sterol
Span
Span ʧˮɽ洼֬
Span 80 ɽ̹
Specific acid-base catalysis ר
Specific surface area ر
Specific surface area method ر
Specific volume ɱȿ
Spermaceti
Spirits
Spongia, spongc
Spray congealing ᷨ
Spray drying
SS
Stability ȶ
Starch
Starch glycolate (CMS-Na) ʴ
state food and drug administration SFDA
STDHF ţ˫ֶ
Sterility
Sterilization
Sticky powder ճԷ
Stocks diameter Stocks
Stokes ٶ
Stratum granulosum
Stratum lucidum
Stress Ӧ
Stress relaxation Ӧ
Stress testing Ӱ顢ǿ
Striping of stratum corneum ȥʲ
Subcutaneous (SC) route Ƥע
Sublingual tablets Ƭ
Subnanoemulsion
Sugar Ƿ
Sugar coated tablets Ƭ
Supercritical Fluid (SCF) ٽ壨ȡ
Suppositories ˨
Surelease һάˮɢ
Surface basis
Suspending agents
Suspensions
Sustained release tablets Ƭ
Sustained-release preparation Ƽ
SUVs С֬
Synergists Эͬ
synthesis of bioconvertible Prod תǰҩĺϳ
Synthesis of lipophilic analogs ֬ʵĺϳ
Synthesis of prodrugs ǰҩĺϳ
Syrups ǽ
Tablets Ƭ
Tacking strength ճ
Talc ʯ
Tap density ʵܶ
Targeting drug system (TDS) ҩϵͳ
TDDS Ƥϵͳ
TDDS ҩᆳƤϵͳ
TDDS Ƥϵͳ
TEM 羵
TEM 羵
Tensile strength (Ts) ǿ
The technique of sterilization
Theory of depletion stabilization ȱȶ
Thermal energy ܷ
Thixlotropy
Thumb tack test Ĵָʵ
Time clock ʱ
Time controlled explosive system ʱ-ͻϵͳ
Tincture
Tincture
Titer ζ
Topochemical reactions ֲѧӦ
Toroches ںƬ
Transdermal therapeutic system
Transfersome
True density ܶ
TTS ƤƼ
Tween ϩʧˮɽ洼֬
Under distribution ɸ·ֲ
Uniform design
Uppsala
UV
Vaginal tablets Ƭ
Vander walls »
Vaselin ʿ
Vertebra caval route ǻע
viscoelasticity ճ
Viscosity ճ
Viscosity ճ
Viscosity coefficient ճϵ
Viscosity curve ճ
Void ratio ϶
Volume basis
Wagner-Nelson ѪҩŨ-ʻ
Watch glass method ƬͷŶȼ飩
Water ˮ
Wet bulb temperature ʪ¶
Wet granulation ʪ
Wetting ʪ
Wool fat ë֬
Wool fat anhydrous ˮë֬
Yield value ֵ
-CYD
OT
CMC-Na ȼά
SG ϩӲ֬
黯OP ϩ20¹
黯SE-10 ϩ10ɽ洼
1-NMP N-ͪ
2G--CYD ǻ
2-HP--CYD 2DZ
5-NCP 5-Ȼͪ
5-NMP 5-ͪ
Accelerated testing
Acrylic acid resin ϩ
Active targeting preparation Ƽ
Adersive dispersion-type TTS ճɢTTS
Adhersive strength ճ
Adhesion ճ
Adhesives ճϼ
Aerosil ۹轺
Aerosol
Aerosol of micropowders for inspiration
Aethylis oleas
Agglomerate ۽
Aggregation ۼ
Air suspension
Alarm clock
Alcohol Ҵ
All-trans ȫʽ
Alterntae addition method ཻ뷨
Amebocyte lysate ϸܽ
Amorphous forms
Angle of repose ֹ
Antiadherent ճ
Antioxidants
Antisepesis
Apparent solubility ܽ
Aprotinin ̪ø
Aquacoat һάˮɢ
Aromatic waters ˮ
Arrhenius ˹
Ascabin ᡡ
Aseptic technique
Azone ͪ
Azone ͪ
Ball mill ĥ
Base adsorption
Bases
Beeswax
Bending
BHA 嶡ǻ
BHT 嶡Լ
Bioavailability ö
Biochemical approach ѧ
***aceutics ҩѧ
Biotechnology \
Bondѧ˵ еȷ飨
Bound water ˮ
Breakage (Bk)
Brij ϩ֬
Brij ϩ֬
Buccal tablets նƬ
Bulk density ܶ
Bulk density ܶȡܶ
Burst effect ͻЧӦ
CA ά
CAB άض
Cabomer ǻϩ
Caking
CAP ά̪
CAP ڱά
CAP ڱά
CAP ڱά
CAP ڱά
Capillary state ëϸ״
Capsules Ҽ
Carbomer ķȻϩ
Carbopol
Carbopol 934
Carboxymethyl cellulose sodium Ǽά
Carboxymethyl starch sodium CMS-Naȼ
Carboxymethylcellulose sodium CMC-Naȼά
CAT άر
CD Բɫ
Cellulose acetate (CA) ά
Cellulose acetate phthalate (CAP) ά̪
Central composite design (CCD) ǵ
Cera aseptical pro osse bone wax
Ceramide
Cetomacrogol Ҷʮ
Chemical approach ѧ
Chewable tablets Ƭ
Chitin Ƕ
Chitosan Ǿ
Chronopathology ʱѧ
Chronopharmacology ʱҩѧ
Clausius-Clapeyron ˹
Clinical pharmaceutics ٴҩѧ
Cloud point ԾϩͷӱԼ
CMC-Na ȼά
CMC-Na ȼά
CMC-Na Ǽά
CMEC ȼά
CMS ȼ
CMS-Na ȼ
Coadminiatration of skin Meta Inh ƤлƼĺ
Coadministraition of chem. P Enh ѧմٽĺ
Coagulation ۳
Coated tablets Ƭ
Coating material
Cocoa butter ɿɶ֬
Cohesion ԡճ
Cohesive strength ھ
Cold compression method ѹ
Cold-homogenization ȴһȻ
Colon-targeted capsules ᳦Ҽ
Compactibility
Complex coacervation ۷
Compliance ˳Ӧ
Compliance ˳Ӧ
Compressed tablets ͨƬ
Compressibility ѹ
Compressibility ѹ
Compression ѹ
Compressive work ѹ
Cone and plate viscometer Բƽճȼ
Consistency curve
Controllability ɿ
Controlled release tablets Ƭ
Controlled-release preparation Ƽ
Convective mixing
Convective transport
Coordination number λ
Copoly (latic/glycolic) acid ҴṲ
Core material
Cosolvency DZ
Cosolvency DZ
Cosolvent DZܼ
Cosolvent DZܼ
Coulter counter method ؼ
Count basis
CP ϩ
CPVP ϩȿͪ
CRacemization
Creams
Creep
Cremolphore EL ϩ
Critical relative humidity (CRH) ٽʪ
Critical relative humidityCRH ٽʪ
Critical velocity ٽٶ
Critrical micell concentration CMCٽ罺Ũ
Croscarmellose sodium CCNaȼά
Croscarmellose sodium (CCNa) ά
Crospovidone άͪ
Cross-liked polyvinyl pyrrolidone PVPPάͪ
Crushing
Crystal form
Crystal habit ̬ᾧϰ
CTS ͨ˨
Cumulative size distribution ۻֲ
Cutting
Cyclodextrin (CYD)
Cylinder model Բ˨ģ
Cytotoxicity ϸ
DDS ҩﴫϵͳ
Decoction
Degree of circularity Բζ
Degree of sphericility ζ
Delipidization ʲȥ֬ʻ
Dextrin
Dialysis cell method ط
Dicetyl phosphate ֬
Dielectric constant 糣
Differential scanning calorimetry DSCʾɨȷ
Differential thermal analysis DTAʾȷ
Diffusive mixing ɢ
Dilatant flow
Diluents ϡͼ
Dimethicone (silicones) ͪ͡͡
Dimethyl sulfoxide(DMSO)
Dimethylacetamide (DMA)
Disinfection
Disintegrants
Disk assemble method Բ̷
Disperse medium ɢ
Disperse phase ɢ
Disperse system ɢϵ
Dispersed phase ɢࡢࡢ
Dispersible tablets ɢƬ
Displacement value (DV) û
Distilled water ˮ
DL-phenylalanine ethyl acetoacetate DL
DLVO
DME
DMSO Ƿ
DM--CYD
Donor cell
DOPE ֬Ҵ
DOPE ֬Ҵ
Dosage form ҩ
DPPC ֬
DPPC ֬
Drop dentifrices
Drug carrier ҩ
Drug-loading rate ҩ
Dry bulb temperature ¶
DSPC Ӳ֬֬
DSPE Ӳ֬֬Ҵ
Dumping effect ͻЧӦ
EA һά
Ear drops ζ
EC һά
EC ëϸܵӾ
EC һά
EC һά
EC һά
EC һά
Effect diameter Dsk,Ч
Effectiveness Ч
Effervescent disintegrants ڱ
Effervescent tablets Ƭ
Elastic deformation Ա
Elastic recovery (ER) Ըԭ
Elastic work Թ
Elasticity
Electro phoresis Ӿ
Electroporesis ¿
Electuary
EMA ױϩ
Emolphor ϩͻ
Emulsifer in water method ˮ黯ʪ
Emulsifier in oil method 黯ɽ
Emulsion ͨ
Emulsions
Enamine ϩ
Endocytosis څ
Endotoxin ڶ
Enteric capsules ܽҼ
Enteric coated tablets Ƭ
Entrapment rate
Epidermis Ƥ
Epimerization 칹
EPRЧӦ
Equilibrium solubility ƽܽ
Equilibrium water ƽˮ
Equivalent specific surface DSV
Equivalent volume diameter Dvȼ۾൱
Ethanol Ҵ
Ethical (prescription) drug ҩ
Ethycellulose (EC) һά
Ethylcellulose ECһά
Ethylene vilnylacetate copolymer ϩ-ϩ
Ethylene vinylacetate copolymer ϩϩ
Eu L, Eu S ۼϩ
Eu RL, Eu RS ۼϩ
Eu RL100, Eu RS100 ϩܣ
Eu RL100, Eu SL100 ۱ϩ֬ϵ
Eu S100, Eu L100 ϩṲܣ
Eudragit (E, RL, RS) ϩ
Eudragit L100 ϩṲ
Eudragit RS100, RL100, NE30D ϩṲ-
Eudragit S100 ϩṲ
EVA ϩϩ
EVA ϩϩ
EVA ϩ-ϩ
EVA ϩ-ϩ
Evaporation
Excipients (adjuvants)
External phase ɢʡࡢ
Extracts
Eye drop ۼ
Eye ointments ۸
Factorial design
Fatty oils ֬
Feret diameter ߾
Ficksһɢʽ ҩȡ
Fillers
Film coated tablets ĤƬ
Film dispersion method ɢ
Films Ĥ
First-pass effect ЧӦ
Fliud extracts
Flocculation
Flocculation
Flocculation value
Flow curve
Flow velocity ٶ
Flowability
Fluid-energy mills ĥʽ
Fluidity buffer Ի
Fluidized bed coating ·
Free water ˮ
Freely movable liquid Һ
Freon ࡢﰺ
Frequency size distribution Ƶʷֲ
Funicular state ״
Fusion ں
Fusion method ӷ
Garles
GAS 巴ܼ
Gas adsorption method
Gas antisolution GAS
Gas permeability method
GCP ҩٴ淶
Gelatin ֽ
Gelatin
Gelatin glycerin ֽ
Gelatinization
General acid-base catalysis
Geometric diameter ѧӾ
Geometric isomerization 칹
Ghost cell Ӱϸ
Glidants
GLP ҩٴо淶
Glycerin
Glycerins ͼ
Glyceryl monostearate Ӳ֬ᡢ
Glycolic acid ǻ
GMP ҩƷ淶
Granule density ܶ
Granules
Graton-Fraserģ ģ
Group number HLB
Guest molecules ͷ
G--CYD ǣ
Half life ˥
Handerson-Hasselbachʽ ״̬pkcphĹϵ
Hard capsules ӲҼ
Hardness Ӳ
HCO DZ
HEC һά
HEMA ϩ
HES һ
Heywood diameter DhͶӰԲ൱
Higuchi ϣ
Host molecules
HPC DZά
HPC DZά
HPMA DZױϩ
HPMC DZά
HPMC DZά
HPMC DZά
HPMC DZά
HPMC DZά
HPMCAS DZά
HPMCAS DZά
HPMCAS DZά
HPMCP DZά̪
HPMCP DZάء
HPMCP Ǽά̪
HPMCP (HP-50, HP-55) DZά
Humidity ʪ
Hydration of stratum corneum ʲˮ
Hydrogel ˮ
Hydrophile-lipophile balance ˮƽֵ
Hydrotropy
Hydrotropy agent ܼ
Hydroxypropyl methylcellulose DZά
Hydroxypropyl methylcellulose acetate succinate DZά
Hydroxypropyl methylcellulose phthalate DZά̪
Hydroxypropylcellulose (HPC) DZά
Hydroxypropylcellulose (HPC) DZά
Hydroxypropylmethyl cellulose HPMCDZά
Hygroscopicity ʪ
Hypodermic tablets ƤעƬ
ICH Э
ICH Э
IDDS ֲҩϵͳ
IEC ӽɫ
IEF ȵ۽
Immobile liquid Һ
Impact
Impact mill ʽ
Implant tablets ֲƬ
Inclusion compound
Industrial pharmaceutics ҵҩѧ
Infusion solution Һ
Injection עҺ
In-liquid drying Һи黯ܼӷ
Interface polycondensation ۷
intra-arterial route ע
Intradermal (ID) route Ƥע
Intramuscular (IM) route ע
Intravenous (IV) route ע
Intrinsic dissolution rate ܳ
Intrinsic solubility ܽ
Inverse targeting
Iontophoresis
IR
Isoclectric focusing IEFȵ۽
Isoosmotic solution Һ
Isopropylpalmitate
Isostearylisostearate Ӳ֬Ӳ
Isotonic solution Һ
Isotonic solution Һ
Journal of Drug Targeting ҩ־
Kickѧ˵ ַ飨
Krafft point ͱԼ
Krummbein diameter
Lactic acid
Lactose
Lag time ʱ
Large unilamellar vesicles ֬
Laurocapam ¹ͪ
Length basis Ȼ
L-HPC ȡDZά
L-HPC ȡDZά
Limulus lysate test 鷨
Liniments
Liposomes ֬
Liquid immersion method Һ
Liquid injection Һע
Liquid paraffin Һʯ
Liquid paraffin ҺʯF
Long-circulating liposome ѭ֬
Long-circulating liposomes ѭ֬
Long-term testing
Loo-Rigelman ˫ѪҩŨȣʻ
Lotions ϴ
Lubricants
Lubricants
LUVs ֬
Martin diameter ȷ־
Mass basis
Matrix type Ǽ
Matrix-diffusion type TTS θɢTTS
Maximum additive concentration MACŨ
MC ά
MC ά
MC ά
MCC ά
Mechanical interlocking bonds ӼеǶ
Medicinal liquor Ƽ
Melt-homogenization ڣȻ
Membrane wall Ĥڿ
Membrane-moderated type TTS ĤTTS
Methyl acrylate-methacrylate co ϩ-ϩ
Methylcellulose (MC) ά
Methylcellulose (MC) ά
Micellar emulsion
Micelle
Microcapsules
Microcrystalline cellulose (MCC) ά
Microcrystalline cellulose (MCC) ά
Microemulsion
Microemulsion
Microencapsulation Ͱ
Micromeritics ѧ
Microreservoir-type TTS
Microscropic method
Microspheres
microstreaming
Minitablet СƬ
Mixing
Mixtures ϼ
MLVs ֬
MMA ϩ
Moistening agent ʪ
Moisture absorption ʪ
Molecular capsules
Multilamellar vesicles ౦֬
Multilayer tablets Ƭ
Multiorfice-centrifugal process ķ
Myrij ϩ֬
Myrj ϩ֬
Nacent soap method
Nanocapsule
Nanocapsules
Nanoemulsion
Nanoemulsion
Nanoliposomes ֬
Nanoparticles
Nanosphere
Nanospheres
Naonparticle
Nasal drops αǼ
Newtonian equation ţճȶ
Newtonian fluid ţ
Niosomes ֬壬
Nonbound water ǽˮ
Nonionic surfactant vesicles ӱԼ
Non-newtonian flow ţ
Non-Newtonian fluid ţ
Nonprescription drug Ǵҩ
Noyes-Whitney ܳٶȷ
NP -ͪ
Nucleation theory ɺ
OCDDS ڷ᳦λҩϵͳ
OCDDS ڷʱ(ʱ)ҩϵͳ
Ointments
Opitical isomerization ѧ칹
ORD ɫɢ
Orthologonal design
Osmotic pressure ѹ
OSSDDS ڷλҩϵͳ
Ostwald freundlich ᾧ
Over the counter (OTC) Ǵҩ
Oversize distribution ɸϷֲ
PA ֬
PACA ϩ
Packing fraction
Paints Ϳ
Paints ͿĤ
Pan coating ·
Paraffin ʯ
Particle size distribution ȷֲ
Partition coefficient (P) ϵ
Passive targeting preparation Ƽ
Patch
PB ۶ϩ
PBCA ϩᶡ
PCS ɢ❪
PE ϩ
PE ϩ
Peel tack test תʵ
PEG Ҷ
PEG Ҷ
PEG Ҷ
PEG-EG PEGε֬Ҵ
Pendular state Ӱ״
Penetration enhancers Ƥմٽ
PEO ϩ
PEO ϩ
PEO ϩ
Peregol O ϩ15ʹ
Perogol O ϩ15ʹ
PET ۶ԱҶ
PG
PGA Ҵ
Pharmaceutical engineering Ƽѧ
Pharmaceutical manufacturing Ƽ
Pharmaceutical preparation ҩƼ
Pharmaceutics ҩѧ
Pharmacia
Pharmacokinetics ҩﶯѧ
Pharmacological availability ҩö
Pharmacopoeia ҩ
Phase inversion critical point תٽ
Phase separation 뷨ѧ
Phase transition temperature תʪ
Phase volume ratio
Phonophoresis
Photodegradation ⻯
PHPMA DZױϩ
Physical and chemical T P ѧƼ
Physical approach ѧ
Physical pharmaceutics ҩѧ
PIB 춡ϩѹ
PiBCA ϩ춡
PiBCA ϩ춡֬
PLA
PLA
PLA
PLA/PGA, PLGA ҽ
PLA-PEG ҶǶι
Plastic deformation Ա
Plastic viscosity ճ
Plastisity
PLGA ҴṲ
PLGA ҽ
PLGA ҴṲ
PMMA ۼϩ
Poiseuile ʽ ʱҺ
Poloxamer (plurnic) ϩϩ
Poloxamer 188 (plurnic F68) ɳķ188F68
Poloxamer 188 (pluronic F68) ɳķ
Poloxamer 188 (Pluronic F68) ɳķ188F68
Poly (lactide-co-glycolide) ۱-ҽ
POLYACRYLICRESIN ۱ϩ
Polyalkylcyano-acrylate ϩ
Polydiethylene terephthalate ۶ԱҶ
Polyethylene ϩ
Polyethylene (PEG) Ҷ
Polyethylene glycol PEGҶ
Polyethylene glycol Ҷ
Polyethylene glycol (PEG) Ҷ
Polyethylene glycol (PEG) Ҷ
Polyethyleneglycol (PEG) Ҷ
Polymerization ۺ
Polymers in pharmaceutics ҩø߷Ӳѧ
Polymethyl methacrylate ۼϩ
Polymorphism ྦྷ
Polymorphism ྦྷ
Polyoxyethylene ϩ
Polyoxyl 40 stearate (Myri52) S-40ϩ40Ӳ֬
Polypropylene ۱ϩ
Polysorbate ɽ
Polyvinyl alcohol ϩ
Polyvinyl alcohol (PVA) ϩ
Polyvinyl chloride ϩ
Polyvinylpyrrolidine PVPάͪ
Polyvinylpyrrolidone άͪ
Porosity ϶
Porosity ϶
Povidone ϩȿͪ
Powder injection δע
Powders ɢ
PP ۱ϩ
PP ۱ϩ
Preformulation ǰ
Pregelatinized starch ۡԤۡѹԵ
Preservative
Pressure sensitive adhersive ѹ
Pressure-sensitive tape council ʵ
Prickle cell layer
Primary particle һ
Prodrug ǰҩ
propellents
Propylene glycol
Propylene glycol (PG)
PS(phosphatidylserine) ֬˿
PSA ѹ
Pseudo steady state α̬
Pseudoplastic flow
PSTC ʵ
Pulsed/pulsatile release ҩ
PVA ϩ
PVA ҽ
PVAP ϩ
PVC ϩ
PVC ϩ
PVC ϩ
PVP άͪ
PVP άͪ
PVP άͪ
PVP (PVPk15, PVPk30, PVPk90) άͪ
PVPP ϩȿͪ
PVPPPVP άͪ
Pycnometer ƿ
Pyrogen ԭ
QOL
Quasi-viscous flow ճ
Racemization
Raman
Random floc
Raoult ڶ
rapid expansion of supercritical S RESS
Rate of shear ٶȡʡٶݶ
Receptor cell ձ
Relative humidity RHʪ
Relative humidity (RH) ʪ
Response surface methodology ЧӦŻ
RESS ٽҺͼ
Retardants ͼ
Reverse osmosis
Rheology ѧ
Rittingerѧ˵ ϸ飨
Rolling ball tack test
RP-HPLC ЧҺɫ
Rubbing ĥ
Rumpf ʪ
SA Ӳ֬
Safety ȫ
Safflower غ컨
SDB-L-400 ۱ϩ
SDS, SLS ʮ
SDS-PAGE SDC۱ϩ
SEC ɫ
Second particle
SEDDSs 黯ҩﴫϵͳ
Sedimentation method
Sedimentation rate ݻ
Self-adjusted system Եʽҩϵͳ
SEM ɨ羵
Sensitization
Settling velocity diameter Ч
SFDA SFDA
Shape factor ״ϵ
Shear mixing л
Shearing force Ӧ
Sieving diameter Daɸ־
Sieving method ɸַ
Sieving method ɸַ
Simple coacervation ۷
Simplex method Ż
Single unilamellar vesicles С֬
Sink condition ©
Sink condition ©״̬
Size exclusion chromatography SEC
Slurry state ཬ̭
Sodium carboxymethyl starch Ǽ
Sodium lauryl sulfate (SDS) ʮջ
Sodium taurodihydrofusidate ţ˫ù
Soft capsules Ҽ
Soft paraffin ʯ
Solid bridges Ӽ
Solid lipid nanospheres (SLN) ֬
Solubility ܽ
Solubility parameter ܽȲ
Solubilization
Solubilization
Solubilization
Solubilizer ܼ
Solubilizer ܼ
Solution tablets ҺƬ
Solutions Һ
Solvent-nonsolvent ܼܼ
SOP
Soybean-derived sterol
Span
Span ʧˮɽ洼֬
Span 80 ɽ̹
Specific acid-base catalysis ר
Specific surface area ر
Specific surface area method ر
Specific volume ɱȿ
Spermaceti
Spirits
Spongia, spongc
Spray congealing ᷨ
Spray drying
SS
Stability ȶ
Starch
Starch glycolate (CMS-Na) ʴ
state food and drug administration SFDA
STDHF ţ˫ֶ
Sterility
Sterilization
Sticky powder ճԷ
Stocks diameter Stocks
Stokes ٶ
Stratum granulosum
Stratum lucidum
Stress Ӧ
Stress relaxation Ӧ
Stress testing Ӱ顢ǿ
Striping of stratum corneum ȥʲ
Subcutaneous (SC) route Ƥע
Sublingual tablets Ƭ
Subnanoemulsion
Sugar Ƿ
Sugar coated tablets Ƭ
Supercritical Fluid (SCF) ٽ壨ȡ
Suppositories ˨
Surelease һάˮɢ
Surface basis
Suspending agents
Suspensions
Sustained release tablets Ƭ
Sustained-release preparation Ƽ
SUVs С֬
Synergists Эͬ
synthesis of bioconvertible Prod תǰҩĺϳ
Synthesis of lipophilic analogs ֬ʵĺϳ
Synthesis of prodrugs ǰҩĺϳ
Syrups ǽ
Tablets Ƭ
Tacking strength ճ
Talc ʯ
Tap density ʵܶ
Targeting drug system (TDS) ҩϵͳ
TDDS Ƥϵͳ
TDDS ҩᆳƤϵͳ
TDDS Ƥϵͳ
TEM 羵
TEM 羵
Tensile strength (Ts) ǿ
The technique of sterilization
Theory of depletion stabilization ȱȶ
Thermal energy ܷ
Thixlotropy
Thumb tack test Ĵָʵ
Time clock ʱ
Time controlled explosive system ʱ-ͻϵͳ
Tincture
Tincture
Titer ζ
Topochemical reactions ֲѧӦ
Toroches ںƬ
Transdermal therapeutic system
Transfersome
True density ܶ
TTS ƤƼ
Tween ϩʧˮɽ洼֬
Under distribution ɸ·ֲ
Uniform design
Uppsala
UV
Vaginal tablets Ƭ
Vander walls »
Vaselin ʿ
Vertebra caval route ǻע
viscoelasticity ճ
Viscosity ճ
Viscosity ճ
Viscosity coefficient ճϵ
Viscosity curve ճ
Void ratio ϶
Volume basis
Wagner-Nelson ѪҩŨ-ʻ
Watch glass method ƬͷŶȼ飩
Water ˮ
Wet bulb temperature ʪ¶
Wet granulation ʪ
Wetting ʪ
Wool fat ë֬
Wool fat anhydrous ˮë֬
Yield value ֵ
-CYD
OT
CMC-Na ȼά
SG ϩӲ֬
黯OP ϩ20¹
黯SE-10 ϩ10ɽ洼