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藥學(xué)英語(yǔ)III山東中醫(yī)藥大學(xué)智慧樹知到答案2024年第一章測(cè)試
Which
of
the
following
parts
of
knowledge
of
drugs
should
be
included
in
pharmacology?
(
)
A:The
effects
of
drugs
on
manB:The
correlation
of
biological
activity
with
chemical
structureC:The
history,
source,
physical
and
chemical
properties,
compounding,
biochemical
and
physiological
effects,
mechanisms
of
action,
absorption,
distribution,
biotransformation
and
excretion.D:The
prevention,
recognition,
and
treatment
of
drug
poisonings.
答案:CWhich
of
the
following
is
what
a
clinician
is
primarily
interested
in
according
to
the
text?
(
)
A:Drugs
which
help
resolve
the
continuing
abuse
of
drug.B:Drugs
which
are
useful
in
the
prevention,
diagnosis
and
treatment
of
human
disease,
or
in
the
prevention
of
pregnancy.C:Chemical
agents
that
are
not
used
in
therapy
but
are
commonly
responsible
for
household
and
industrial
poisoning
as
well
as
environmental
pollution.D:Drugs
which
can
be
reasonably
limited
to
those
aspects
that
provide
the
basis
for
their
rational
clinical
use.
答案:BWhy
was
the
physician
not
interested
in
pharmacognosy?
(
)
A:Natural
drugs
had
little
difference
with
synthetic
onesB:He
had
a
broad
botanical
knowledgeC:Fewer
drugs
were
obtained
from
natural
sourcesD:He
didn't
have
to
select
the
proper
plants
for
his
prescription.
答案:AWhich
of
the
following
is
the
best
way
of
studying
pharmacology
for
medical
students
and
practitioners?
(
)
A:to
select
a
plant
and
its
preparationB:to
have
the
ability
to
purify
natural
plantsC:to
have
a
broad
botanical
knowledgeD:to
have
curiosity
that
stimulates
them
to
learn
about
sources
of
drugs
答案:DWhat
are
the
tasks
related
to
medicines
almost
completely
delegated
to
the
pharmacists
now?
(
)
A:the
preparing,
compounding,
and
dispensing
of
medicinesB:the
physical
and
chemical
properties
of
medicinesC:the
therapeutic
and
other
uses
of
medicinesD:dosage
forms
of
medicines
available
答案:A
第二章測(cè)試
H.
Mario
Geysen
initially
used
parallel
synthesis
as
a
quick
way
to
identify
which
small
(
)
of
any
given
large
protein
bound
to
an
antibody.
A:partB:FragmentC:divisionD:pieces
答案:CChemists
often
start
a
combinatorial
synthesis
by
attaching
the
first
set
of
building
blocks
to
(
),
microscopic
beads
made
of
polystyrene.
A:solid
B:ActiveC:softD:inert
答案:CThe
chemical
reactions
required
to
link
compounds
to
the
beads
and
later
to
detach
them
(
)
to
the
synthesis
process.
A:introduce
complicationsB:make
easyC:introduce
easyD:induce
complications
答案:BIn
a
parallel
synthesis,
all
the
products
are
(
)
separately
in
their
own
reaction
vessels.
A:assembledB:AssortedC:joinedD:combined
答案:BIn
many
laboratories
today,
robots
assist
with
the
routine
work
of
parallel
synthesis,
such
as
(
)
small
amounts
of
reactive
molecules
into
the
appropriate
wells.
A:deliveringB:transportingC:givingD:sending
答案:C
第三章測(cè)試
Pharmaceutics
is
an
interdisciplinary
subject
involving
(
)
A:manufacturingB:physical
pharmacyC:formulation,
manufacturing,
physical
pharmacy,
and
biopharmaceuticsD:Biopharmaceutics
答案:CFormulation
is
about
the
design,
development
and
evaluation
of
dosage
forms,
(
)
A:analytical
methodsB:discovery
of
novel
drugsC:drug
delivery
systems
and
manufacturing
processD:dosing
regimen
答案:CBiopharmaceutics
mainly
studies
the
in
vivo
process
of
drugs
and
metabolites
in
humans,
animals
and
tissue
culture,
which
specifically
involves
(
)
A:absorption
and
excretionB:absorption
and
distributionC:metabolism
and
excretionD:absorption,
distribution,
metabolism,
and
excretion
答案:DRegarding
the
definition
of
bioavailability
(BA),
BA
is
related
to
(
)
A:total
plasma
drug
concentration,
and
the
administered
drug
doseB:unbound
drug
concentration
at
the
target
siteC:unbound
drug
concentration
in
the
plasmaD:total
plasma
drug
concentration
only
答案:APlasma
drug
concentration
is
affected
by
following
factors
such
as
(
)
A:all
of
aboveB:rate
of
eliminationC:rate
and
extent
of
distributionD:rate
of
absorption
答案:A
第四章測(cè)試
Blood
(
)
must
be
monitored
in
diabetics
(and,
in
fact,
most
diseases
are
diagnosed
by
chemical
analysis).
A:glucos
B:ProteinC:B
PHD:hemoglobin
答案:AIn
medicine,
analytical
chemistry
is
the
basis
for
(
)
laboratory
tests
which
help
physicians
diagnose
disease
and
chart
progress
in
recovery.
A:clinicalB:FuelC:agriculturalD:polymer
答案:AIn
industry,
analytical
chemistry
provides
the
means
of
testing
raw
materials
and
for
assuring
the
quality
of
finished
products
whose
chemical
(
)
is
critical.
A:compoundB:concentrationC:ClassD:composition
答案:D(
)
quality
is
often
evaluated
by
testing
suspected
contaminants
using
the
techniques
of
analytical
chemistry.
A:NutritionalB:EngineeringC:EnvironmentalD:Agricultural
答案:CThe
formation
of
a
white
precipitate
when
adding
a
solution
of
silver
nitrate
to
a
dissolved
sample
indicates
the
presence
of
(
).
A:sulfideB:nitrateC:chlorideD:Sulfate
答案:C(
)
spectra
will
give
"fingerprints"
of
organic
compounds
or
their
functional
groups.
A:MassB:VisibleC:InfraredD:Ultraviolet
答案:CChromatography
provides
powerful
(
).
A:precipitationB:instrumentationC:extractionD:Separation
答案:DThe
list
of
prohibited
substances
at
the
Olympic
Games
includes
about
500
different
active
constituents,
such
as
(
).
A:stimulantsB:beta-blockersC:all
of
the
aboveD:steroids
答案:CDoped
compounds
are
identified
using
the
highly
selective
combination
of
gas
(
)-mass
spectrometry
(GC-MS).
A:ChromatographyB:concentrationC:phaseD:flow
答案:A(
)
spectrometry
provides
molecular
structural
data
on
the
compounds.
A:MassB:UltravioletC:InfraredD:Visible
答案:A
第五章測(cè)試
What
is
the
meaning
of
HTS?
(
)
A:High
Temperature
SuperconductingB:Heat
Transfer
SaltsC:High
Throughput
ScreeningD:Heat-treated
Steel
答案:CWhat
category
does
simvastatin
belong
to?
(
)
A:antibiotics
of
aminoglycosidesB:AnalgesicsC:antineoplastic
agentsD:lipid
regulating
agents
答案:DWhat
category
does
paclitaxel
belong
to?
(
)
A:antibiotics
of
aminoglycosidesB:AnalgesicsC:lipid
regulating
agentsD:antineoplastic
agents
答案:DWhat
category
does
azithromycin
belong
to?
(
)
A:lipid
regulating
agentsB:antibiotics
of
macrolidesC:antineoplastic
agentsD:analgesics
答案:B90%to95%of
plants
on
this
planet
have
not
been
investigated
so
far.
(
)
A:錯(cuò)B:對(duì)
答案:BTo
incorporate
natural
products
in
the
modern
HTS
programmes,
a
natural
product
library
is
not
useful.
(
)
A:對(duì)B:錯(cuò)
答案:BNatural
products
have
been
a
source
of
drugs
and
drug
leads.
(
)
A:對(duì)B:錯(cuò)
答案:AThe
traditional
way
of
discovering
drug
from
natural
product
is
bioassay-guided.
(
)
A:對(duì)B:錯(cuò)
答案:AAcademia
and
some
semi-academic
research
organizations
usually
apply
modern
approaches
to
natural
product
drug
discovery.
(
)
A:對(duì)B:錯(cuò)
答案:BCephalosporin
C
is
an
antiviral
compound.
(
)
A:對(duì)B:錯(cuò)
答案:B
第六章測(cè)試
(
)
is
generally
directly
related
to
uncertainty
and
is
reduced
through
knowledge
and
best
scientific
practices.
A:SafetyB:ImmunogenicityC:SpecificityD:Efficacy
答案:ABecause
of
the
(
)
of
the
compound
class,
our
future
nonclinical
development
programs
must
be
considered
largely
on
a
case-by-case
basis.
A:specificity
B:toxicityC:SafetyD:heterogeneity
答案:DAdequate
exposure
needed
for
specific
treatment
regimens
can
be
hindered
by
the
formation
of
(
)
with
drug
neutralization
or
accelerated
clearance.
A:antigensB:CytokinesC:antibodies
D:antidrug
antibodies
答案:DToxicology
programs
with
(
)
administration
of
biologics
often
have
less
long-term
treatments
than
SMDS.
A:properB:single-dose
C:large-doseD:multiple-dose
答案:DAs
in
the
case
for
small
molecules,
some
toxicological
studies
have
to
be
performed
before
first
use
in
humans.
(
)
A:錯(cuò)B:對(duì)
答案:ASmall
molecules
generally
do
not
necessarily
need
a
PK
assay
for
quantification
of
the
unchanged
compound
and
its
(major)
metabolite(s).
(
)
A:錯(cuò)B:對(duì)
答案:Asample-clean
procedures
routinely
used
for
small
molecules
cannot
usually
be
used
for
biologics.
(
)
A:對(duì)B:錯(cuò)
答案:AEssential
reagents
such
as
poly-
or
monoclonal
antibodies
might
not
be
difficult
to
obtain
in
the
early
stages
of
development.
(
)
A:錯(cuò)B:對(duì)
答案:AThe
activity
assay
is
particularly
useful
for
measuring
the
neutralizing
activity
of
an
ADA,
although
it
was
originally
developed
to
measure
product
efficacy.
(
)
A:對(duì)B:錯(cuò)
答案:ATissue
cross-reactivity
(TCR)
studies
in
a
panel
of
human
tissues
determining
the
level
of
cross-recognition
are
necessary
for
targeted
biologics
such
as
mAbs.
(
)
A:對(duì)B:錯(cuò)
答案:A
第七章測(cè)試
(
)
increases
risk
of
bleeding.
A:Excessive
coagulationB:Insufficient
anticoagulationC:Insufficient
warfarinD:Excessive
warfarin
答案:DWhich
of
the
following
statements
is
TRUE?
(
)
A:A
drug
will
certainly
be
efficacious
in
actual
use
if
it
was
already
proved
in
clinical
trials.B:A
drug
that
is
proved
effective
in
a
clinical
trial
will
have
similar
effectiveness
in
actual
use.C:Drugs
that
are
efficacious
in
clinical
trials
may
not
be
very
effective
in
clinical
uses.D:A
drug
that
is
efficacious
in
clinical
trials
will
always
be
not
very
effective
in
actual
use.
答案:CWhich
of
following
elements
is
not
involved
in
Patient-oriented
outcomes?
(
)
A:concentrations
of
cholesterolB:relief
of
symptomsC:prevention
of
disabilityD:prolongation
of
life
答案:AClinicians
often
consider
factors
that
are
somewhat
(
),
such
as
personal
experience,
anecdotes,
peer
practices,
and
expert
opinions.
A:objectivelyB:objectiveC:subjectivelyD:subjective
答案:DThe
intuitive
standard
used
for
the
measurement
of
efficacy
and
safety
in
medical
history
are
no
longer
used
today.
(
)
A:對(duì)B:錯(cuò)
答案:BUnlike
effectiveness,
efficacy
cannot
be
evaluated
accurately
even
in
an
ideal
environment.
(
)
A:對(duì)B:錯(cuò)
答案:BSurrogate
outcomes
are
preferred
measures
of
efficacy
than
patient-oriented
outcomes,
because
they
can
be
much
more
feasible
to
use.
(
)
A:錯(cuò)B:對(duì)
答案:AAdverse
effects
may
only
be
fully
known
after
a
drug
has
been
in
widespread
clinical
use
for
a
long
time.
(
)
A:錯(cuò)B:對(duì)
答案:BEven
a
drug
that
causes
many
more
harms
than
benefits,
it
may
still
be
worth
prescribing
to
patients.
(
)
A:錯(cuò)B:對(duì)
答案:BA
drug
with
wide
therapeutic
window
is
often
safer
than
those
with
narrow
ones.
(
)
A:錯(cuò)B:對(duì)
答案:B
第八章測(cè)試
(
)
is
the
drug
regulatory
agency
in
the
UK.
A:CFDAB:MHRAC:FDAD:EMA
答案:BWhich
of
the
following
statements
about
the
US
and
the
UK
requirements
on
GMP
is
NOT
true?
(
)
A:The
US
required
all
drugs
should
be
manufactured
according
to
GMP
requirementsB:The
US
GMP
has
the
force
of
lawC:The
UK
GMP
was
mandatoryD:The
UK
only
inspected
drug
products
and
biological
manufacturers
答案:CWhich
of
the
following
statements
on
the
manufacture
of
API
is
NOT
true?
(
)
A:The
manufacturing
processes
involve
purification
at
each
stageB:An
API
is
normally
prepared
by
chemical
processesC:Impurities
present
in
final
API
will
be
removedD:The
impurities
in
API
will
not
influence
the
quality
of
drug
product
答案:C“Starting
material”
includes
(
)
A:both
A
and
BB:raw
materialC:excipientsD:paIckaging
material
答案:AGMP
compliance
is
a
requirement
only
for
the
manufacture
of
drug
products.
(
)
A:對(duì)B:錯(cuò)
答案:BAccording
to
FD&C
Act,
only
drug
products
shall
be
manufactured
in
accordance
with
cGMP.
(
)
A:錯(cuò)B:對(duì)
答案:AICH
Q7
A
is
a
worldwide
guidance
for
the
manufacture
of
drug
products
for
both
commercial
and
R&D
purposes.
(
)
A:錯(cuò)B:對(duì)
答案:BSame
as
that
in
the
USA,
all
drug
products
are
inspected
by
the
regulatory
authority
for
compliance
to
GMP
in
the
UK.
(
)
A:錯(cuò)B:對(duì)
答案:AImpurities
in
the
final
API
will
be
removed
because
it
will
influence
the
quality
of
drug
products.
(
)
A:對(duì)B:錯(cuò)
答案:BEach
stage
of
A
PI
production
will
influence
the
quality
of
final
API.
(
)
A:錯(cuò)B:對(duì)
答案:A
第九章測(cè)試
Which
of
the
following
statements
is
right
according
to
the
passage?
(
)
A:There
is
a
relationship
between
the
significance
of
the
contraindications
and
the
likelihood
of
occurrence
and
the
size
of
population.B:Adverse
reaction
is
usually
included
in
Highlights
of
Prescribing
Information
section.C:That
there
are
no
known
contraindications
for
a
drug
means
therapeutical
benefits
outweigh
risks.D:Both
known
dangers
and
theoretical
possibilities
should
be
listed
in
“Contraindications”.
答案:AIn
a
drug
insert,
pharmacokinetic
effects
are
included
in
(
)
section
A:Recent
Major
ChangesB:ContraindicationsC:Drug
InteractionD:FPI
Contents
答案:CSome
information
in
FPI
Contents
section
is
cross-referenced
in
(
)
section.
A:Highlights
of
Prescribing
InformationB:ContraindicationsC:Black
Box
WarningD:Warnings
and
Precautions
答案:AWhen
the
ADR
requires
adjusting
drug
dosage
or
regimen,
discontinuing
the
drug
and
evaluating
the
patient
for
medication
compliance,
it
means
that
the
ADR
associated
with
use
of
the
drug
is
(
).
A:clinically
insufficientB:clinically
sufficientC:clinically
significantD:clinically
insignificant
答案:CIn
the
1980s,
health
practitioners
found
i
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