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藥學(xué)英語(yǔ)III智慧樹(shù)知到課后章節(jié)答案2023年下山東中醫(yī)藥大學(xué)山東中醫(yī)藥大學(xué)
第一章測(cè)試
Which
of
the
following
parts
of
knowledge
of
drugs
should
be
included
in
pharmacology?
(
)
A:The
correlation
of
biological
activity
with
chemical
structureB:The
prevention,
recognition,
and
treatment
of
drug
poisonings.C:The
history,
source,
physical
and
chemical
properties,
compounding,
biochemical
and
physiological
effects,
mechanisms
of
action,
absorption,
distribution,
biotransformation
and
excretion.D:The
effects
of
drugs
on
man
答案:The
history,
source,
physical
and
chemical
properties,
compounding,
biochemical
and
physiological
effects,
mechanisms
of
action,
absorption,
distribution,
biotransformation
and
excretion.
Which
of
the
following
is
what
a
clinician
is
primarily
interested
in
according
to
the
text?
(
)
A:Drugs
which
are
useful
in
the
prevention,
diagnosis
and
treatment
of
human
disease,
or
in
the
prevention
of
pregnancy.B:Chemical
agents
that
are
not
used
in
therapy
but
are
commonly
responsible
for
household
and
industrial
poisoning
as
well
as
environmental
pollution.C:Drugs
which
can
be
reasonably
limited
to
those
aspects
that
provide
the
basis
for
their
rational
clinical
use.D:Drugs
which
help
resolve
the
continuing
abuse
of
drug.
答案:Drugs
which
are
useful
in
the
prevention,
diagnosis
and
treatment
of
human
disease,
or
in
the
prevention
of
pregnancy.
Which
of
the
following
is
the
best
way
of
studying
pharmacology
for
medical
students
and
practitioners?
(
)
A:to
have
curiosity
that
stimulates
them
to
learn
about
sources
of
drugsB:to
have
the
ability
to
purify
natural
plantsC:to
select
a
plant
and
its
preparationD:to
have
a
broad
botanical
knowledge
答案:to
have
curiosity
that
stimulates
them
to
learn
about
sources
of
drugs
What
are
the
tasks
related
to
medicines
almost
completely
delegated
to
the
pharmacists
now?
(
)
A:the
physical
and
chemical
properties
of
medicinesB:the
therapeutic
and
other
uses
of
medicinesC:the
preparing,
compounding,
and
dispensing
of
medicinesD:dosage
forms
of
medicines
available
答案:the
preparing,
compounding,
and
dispensing
of
medicines
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:divisionC:FragmentD:pieces
答案:division
Chemists
often
start
a
combinatorial
synthesis
by
attaching
the
first
set
of
building
blocks
to
(
),
microscopic
beads
made
of
polystyrene.
A:softB:ActiveC:solid
D:inert
答案:soft
The
chemical
reactions
required
to
link
compounds
to
the
beads
and
later
to
detach
them
(
)
to
the
synthesis
process.
A:introduce
easyB:induce
complications
C:make
easyD:introduce
complications
答案:make
easy
In
a
parallel
synthesis,
all
the
products
are
(
)
separately
in
their
own
reaction
vessels.
A:joinedB:AssortedC:assembledD:combined
答案:Assorted
In
many
laboratories
today,
robots
assist
with
the
routine
work
of
parallel
synthesis,
such
as
(
)
small
amounts
of
reactive
molecules
into
the
appropriate
wells.
A:transportingB:sending
C:givingD:delivering
答案:giving
第三章測(cè)試
Pharmaceutics
is
an
interdisciplinary
subject
involving
(
)
A:formulation,
manufacturing,
physical
pharmacy,
and
biopharmaceuticsB:physical
pharmacyC:BiopharmaceuticsD:manufacturing
答案:formulation,
manufacturing,
physical
pharmacy,
and
biopharmaceutics
Formulation
is
about
the
design,
development
and
evaluation
of
dosage
forms,
(
)
A:drug
delivery
systems
and
manufacturing
processB:dosing
regimenC:analytical
methodsD:discovery
of
novel
drugs
答案:drug
delivery
systems
and
manufacturing
process
Biopharmaceutics
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:absorption,
distribution,
metabolism,
and
excretionD:metabolism
and
excretion
答案:absorption,
distribution,
metabolism,
and
excretion
Regarding
the
definition
of
bioavailability
(BA),
BA
is
related
to
(
)
A:unbound
drug
concentration
at
the
target
siteB:total
plasma
drug
concentration
onlyC:total
plasma
drug
concentration,
and
the
administered
drug
doseD:unbound
drug
concentration
in
the
plasma
答案:total
plasma
drug
concentration,
and
the
administered
drug
dose
Plasma
drug
concentration
is
affected
by
following
factors
such
as
(
)
A:all
of
aboveB:rate
and
extent
of
distributionC:rate
of
absorptionD:rate
of
elimination
答案:all
of
above
第四章測(cè)試
Blood
(
)
must
be
monitored
in
diabetics
(and,
in
fact,
most
diseases
are
diagnosed
by
chemical
analysis).
A:hemoglobinB:ProteinC:B
PHD:glucos
答案:glucos
In
medicine,
analytical
chemistry
is
the
basis
for
(
)
laboratory
tests
which
help
physicians
diagnose
disease
and
chart
progress
in
recovery.
A:FuelB:clinicalC:polymerD:agricultural
答案:clinical
In
industry,
analytical
chemistry
provides
the
means
of
testing
raw
materials
and
for
assuring
the
quality
of
finished
products
whose
chemical
(
)
is
critical.
A:concentrationB:compoundC:compositionD:Class
答案:composition
(
)
quality
is
often
evaluated
by
testing
suspected
contaminants
using
the
techniques
of
analytical
chemistry.
A:EnvironmentalB:AgriculturalC:NutritionalD:Engineering
答案:Environmental
The
formation
of
a
white
precipitate
when
adding
a
solution
of
silver
nitrate
to
a
dissolved
sample
indicates
the
presence
of
(
).
A:sulfideB:chlorideC:nitrateD:Sulfate
答案:chloride
(
)
spectra
will
give
"fingerprints"
of
organic
compounds
or
their
functional
groups.
A:VisibleB:InfraredC:UltravioletD:Mass
答案:Infrared
Chromatography
provides
powerful
(
).
A:SeparationB:precipitationC:extractionD:instrumentation
答案:Separation
The
list
of
prohibited
substances
at
the
Olympic
Games
includes
about
500
different
active
constituents,
such
as
(
).
A:stimulantsB:steroidsC:all
of
the
aboveD:beta-blockers
答案:all
of
the
above
Doped
compounds
are
identified
using
the
highly
selective
combination
of
gas
(
)-mass
spectrometry
(GC-MS).
A:concentrationB:flowC:phaseD:Chromatography
答案:Chromatography
(
)
spectrometry
provides
molecular
structural
data
on
the
compounds.
A:UltravioletB:MassC:InfraredD:Visible
答案:Mass
第五章測(cè)試
What
is
the
meaning
of
HTS?
(
)
A:High
Throughput
ScreeningB:Heat-treated
SteelC:High
Temperature
SuperconductingD:Heat
Transfer
Salts
答案:High
Throughput
Screening
What
category
does
simvastatin
belong
to?
(
)
A:lipid
regulating
agentsB:AnalgesicsC:antineoplastic
agentsD:antibiotics
of
aminoglycosides
答案:lipid
regulating
agents
What
category
does
paclitaxel
belong
to?
(
)
A:antineoplastic
agentsB:antibiotics
of
aminoglycosidesC:lipid
regulating
agentsD:Analgesics
答案:antineoplastic
agents
What
category
does
azithromycin
belong
to?
(
)
A:lipid
regulating
agentsB:antibiotics
of
macrolidesC:antineoplastic
agentsD:analgesics
答案:antibiotics
of
macrolides
90%to95%of
plants
on
this
planet
have
not
been
investigated
so
far.
(
)
A:對(duì)B:錯(cuò)
答案:對(duì)
To
incorporate
natural
products
in
the
modern
HTS
programmes,
a
natural
product
library
is
not
useful.
(
)
A:對(duì)B:錯(cuò)
答案:錯(cuò)
Natural
products
have
been
a
source
of
drugs
and
drug
leads.
(
)
A:對(duì)B:錯(cuò)
答案:對(duì)
The
traditional
way
of
discovering
drug
from
natural
product
is
bioassay-guided.
(
)
A:錯(cuò)B:對(duì)
答案:對(duì)
Academia
and
some
semi-academic
research
organizations
usually
apply
modern
approaches
to
natural
product
drug
discovery.
(
)
A:對(duì)B:錯(cuò)
答案:錯(cuò)
Cephalosporin
C
is
an
antiviral
compound.
(
)
A:對(duì)B:錯(cuò)
答案:錯(cuò)
第六章測(cè)試
(
)
is
generally
directly
related
to
uncertainty
and
is
reduced
through
knowledge
and
best
scientific
practices.
A:SafetyB:EfficacyC:ImmunogenicityD:Specificity
答案:Safety
Because
of
the
(
)
of
the
compound
class,
our
future
nonclinical
development
programs
must
be
considered
largely
on
a
case-by-case
basis.
A:toxicityB:heterogeneityC:specificity
D:Safety
答案:heterogeneity
Adequate
exposure
needed
for
specific
treatment
regimens
can
be
hindered
by
the
formation
of
(
)
with
drug
neutralization
or
accelerated
clearance.
A:antidrug
antibodiesB:antigensC:CytokinesD:antibodies
答案:antidrug
antibodies
Toxicology
programs
with
(
)
administration
of
biologics
often
have
less
long-term
treatments
than
SMDS.
A:multiple-doseB:single-dose
C:large-doseD:proper
答案:multiple-dose
As
in
the
case
for
small
molecules,
some
toxicological
studies
have
to
be
performed
before
first
use
in
humans.
(
)
A:對(duì)B:錯(cuò)
答案:錯(cuò)
Small
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:錯(cuò)
sample-clean
procedures
routinely
used
for
small
molecules
cannot
usually
be
used
for
biologics.
(
)
A:錯(cuò)B:對(duì)
答案:對(duì)
Essential
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:錯(cuò)
The
activity
assay
is
particularly
useful
for
measuring
the
neutralizing
activity
of
an
ADA,
although
it
was
originally
developed
to
measure
product
efficacy.
(
)
A:錯(cuò)B:對(duì)
答案:對(duì)
Tissue
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:錯(cuò)B:對(duì)
答案:對(duì)
第七章測(cè)試
(
)
increases
risk
of
bleeding.
A:Insufficient
warfarinB:Insufficient
anticoagulationC:Excessive
warfarinD:Excessive
coagulation
答案:Excessive
warfarin
Which
of
the
following
statements
is
TRUE?
(
)
A:A
drug
that
is
proved
effective
in
a
clinical
trial
will
have
similar
effectiveness
in
actual
use.B:A
drug
will
certainly
be
efficacious
in
actual
use
if
it
was
already
proved
in
clinical
trials.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:Drugs
that
are
efficacious
in
clinical
trials
may
not
be
very
effective
in
clinical
uses.
Which
of
following
elements
is
not
involved
in
Patient-oriented
outcomes?
(
)
A:prolongation
of
lifeB:prevention
of
disabilityC:relief
of
symptomsD:concentrations
of
cholesterol
答案:concentrations
of
cholesterol
Clinicians
often
consider
factors
that
are
somewhat
(
),
such
as
personal
experience,
anecdotes,
peer
practices,
and
expert
opinions.
A:objectiveB:subjectivelyC:objectivelyD:subjective
答案:subjective
The
intuitive
standard
used
for
the
measurement
of
efficacy
and
safety
in
medical
history
are
no
longer
used
today.
(
)
A:錯(cuò)B:對(duì)
答案:錯(cuò)
Unlike
effectiveness,
efficacy
cannot
be
evaluated
accurately
even
in
an
ideal
environment.
(
)
A:對(duì)B:錯(cuò)
答案:錯(cuò)
Surrogate
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:錯(cuò)
Adverse
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:對(duì)
Even
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:對(duì)
A
drug
with
wide
therapeutic
window
is
often
safer
than
those
with
narrow
ones.
(
)
A:對(duì)B:錯(cuò)
答案:對(duì)
第八章測(cè)試
(
)
is
the
drug
regulatory
agency
in
the
UK.
A:FDAB:CFDAC:EMAD:MHRA
答案:MHRA
Which
of
the
following
statements
about
the
US
and
the
UK
requirements
on
GMP
is
NOT
true?
(
)
A:The
UK
GMP
was
mandatoryB:The
US
GMP
has
the
force
of
lawC:The
UK
only
inspected
drug
products
and
biological
manufacturersD:The
US
required
all
drugs
should
be
manufactured
according
to
GMP
requirements
答案:The
UK
GMP
was
mandatory
Which
of
the
following
statements
on
the
manufacture
of
API
is
NOT
true?
(
)
A:The
impurities
in
API
will
not
influence
the
quality
of
drug
productB:An
API
is
normally
prepared
by
chemical
processesC:Impurities
present
in
final
API
will
be
removedD:The
manufacturing
processes
involve
purification
at
each
stage
答案:Impurities
present
in
final
API
will
be
removed
“Starting
material”
includes
(
)
A:paIckaging
materialB:raw
materialC:both
A
and
BD:excipients
答案:both
A
and
B
GMP
compliance
is
a
requirement
only
for
the
manufacture
of
drug
products.
(
)
A:錯(cuò)B:對(duì)
答案:錯(cuò)
According
to
FD&C
Act,
only
drug
products
shall
be
manufactured
in
accordance
with
cGMP.
(
)
A:錯(cuò)B:對(duì)
答案:錯(cuò)
ICH
Q7
A
is
a
worldwide
guidance
for
the
manufacture
of
drug
products
for
both
commercial
and
R&D
purposes.
(
)
A:對(duì)B:錯(cuò)
答案:對(duì)
Same
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:錯(cuò)
Impurities
in
the
final
API
will
be
removed
because
it
will
influence
the
quality
of
drug
products.
(
)
A:錯(cuò)B:對(duì)
答案:錯(cuò)
Each
stage
of
A
PI
production
will
influence
the
quality
of
final
API.
(
)
A:錯(cuò)B:對(duì)
答案:錯(cuò)
第九章測(cè)試
Which
of
the
following
statements
is
right
according
to
the
passage?
(
)
A:That
there
are
no
known
contraindications
for
a
drug
means
therapeutical
benefits
outweigh
risks.B:Both
known
dangers
and
theoretical
possibilities
should
be
listed
in
“Contraindications”.C:There
is
a
relationship
between
the
significance
of
the
contraindications
and
the
likelihood
of
occurrence
and
the
size
of
population.D:Adverse
reaction
is
usually
included
in
Highlights
of
Prescribing
Information
section.
答案:There
is
a
relationship
between
the
significance
of
the
contraindications
and
the
likelihood
of
occurrence
and
the
size
of
population.
In
a
drug
insert,
pharmacokinetic
effects
are
included
in
(
)
section
A:ContraindicationsB:Drug
InteractionC:FPI
ContentsD:Recent
Major
Changes
答案:Drug
Interaction
Some
information
in
FPI
Contents
section
is
cross-referenced
in
(
)
section.
A:Highlights
of
Prescribing
InformationB:Warnings
and
PrecautionsC:ContraindicationsD:Black
Box
Warning
答案:Highlights
of
Prescribing
Information
When
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
significantB:clinically
insufficientC:clini
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