Microcrystalline tests for Drug Analysis// A Commendable method equivalent to Instrumental analysis

00:16:52
https://www.youtube.com/watch?v=XQFT35g3n3c

概要

TLDRThe video provides an overview of the micro crystalline test, a significant method for drug identification and verification in forensic science, especially when instrumental analysis is unavailable. It explains the historical context and advantages of the technique, including low cost and specificity. However, it also outlines the limitations, such as its applicability to certain substances and need for expertise in interpretation. Various testing techniques like aqueous and volatility methods are discussed, alongside examples of crystal formations for different drugs. The video emphasizes that while micro crystalline tests are valuable, they have limitations compared to modern instrumental methods.

収穫

  • 🧪 Micro crystalline tests are essential for drug analysis.
  • 💰 They are cost-effective and specific.
  • ⚖️ Limited applicability to substances exists.
  • ⏱️ Fast results can be obtained within minutes.
  • 🔍 Expertise in interpretation is crucial.
  • 🧊 Techniques include aqueous and volatility methods.
  • 🏆 Useful for identifying optical isomers.
  • 🔬 Polarized light microscopy plays a key role.
  • ♻️ Environmentally friendly and less reagent consumption.
  • 📊 Instrumental methods provide more versatile analysis.

タイムライン

  • 00:00:00 - 00:05:00

    In the introduction to the micro crystalline test, it is presented as a commendable alternative to instrumental analysis for drug identification. These methods, which have been in use for over a century, are particularly useful in cases where automated systems are unavailable or results are compromised by mixtures or adulterants. Micro crystalline tests can effectively analyze various drug forms, including gels and transdermal patches, making them especially valuable for small-scale forensic labs that rely heavily on light microscopy. The test utilizes polarized light microscopy for fast and specific identification, which is less expensive compared to other methods while confirming results obtained through alternative methods.

  • 00:05:00 - 00:10:00

    The advantages and limitations of micro crystalline tests are well outlined. They are advantageous as they require minimal equipment and reagents and are environmentally friendly. However, they are not suitable for all substances and can produce multiple crystal formations that complicate identification. Also, contamination of samples can hinder the effectiveness of the test, requiring purification procedures prior to testing. While micro crystalline tests are important analytical methods that contribute to drug identification, they have limitations in versatility and quantization, necessitating skilled interpretation for accurate results.

  • 00:10:00 - 00:16:52

    The techniques used in micro crystalline testing include aqueous techniques and volatility techniques which may involve specific conditions such as temperature control and maintaining pH levels through acids or bases. The process involves the observation of crystal formations by mixing the sample and reagents under the microscope. Additionally, various methods for crystal formation are detailed, including acid anionic tests for specific compounds. Different drugs exhibit specific crystal types under certain reagents, highlighting the test's usefulness in drug identification, yet emphasizing the need for careful analysis due to similar crystal formations across different compounds.

マインドマップ

ビデオQ&A

  • What is the micro crystalline test used for?

    The micro crystalline test is used for drug identification and verification, especially when instrumental methods are not available.

  • What are the advantages of micro crystalline tests?

    Advantages include being inexpensive, highly specific, and environmentally friendly, with minimal reagent consumption.

  • What are the disadvantages of micro crystalline testing?

    Disadvantages include limited applicability to various substances and potential interference from other crystal forming agents.

  • How do micro crystalline tests compare to instrumental methods?

    Micro crystalline tests are less versatile and applicable for few substances, while instrumental methods provide more comprehensive analysis.

  • What techniques are used in micro crystalline testing?

    Techniques include aqueous techniques, volatility techniques, and acid-anionic test techniques.

  • What is necessary for effective micro crystalline testing?

    Expertise and skills in interpreting crystal formations are crucial for accurate results.

  • Can micro crystalline tests identify optical isomers?

    Yes, micro crystalline tests can differentiate optical isomers based on their unique crystal formations.

  • Are there any specific reagents used for the micro crystalline test?

    Yes, specific metal halides are often used as reagents to induce crystal formation.

  • Is sample purification required before testing?

    While purification is generally not required, preprocessing may be necessary if samples are concentrated.

  • What role does polarized light microscopy play in micro crystalline testing?

    Polarized light microscopy is used to examine and differentiate the types of crystals formed.

ビデオをもっと見る

AIを活用したYouTubeの無料動画要約に即アクセス!
字幕
en
オートスクロール:
  • 00:00:01
    welcome back to our channel friends
  • 00:00:02
    foreign public desk india
  • 00:00:04
    today's topic is micro crystalline test
  • 00:00:06
    a commendable method
  • 00:00:08
    equivalent to instrumental analysis
  • 00:00:10
    let's proceed further
  • 00:00:12
    introduction to micro crystalline test
  • 00:00:15
    traditional light microscopy
  • 00:00:16
    and micro crystal tests
  • 00:00:20
    are very old and used since more than
  • 00:00:23
    100 years
  • 00:00:24
    these are proven useful when automated
  • 00:00:27
    instrumental analysis are not available
  • 00:00:29
    or the results are not appropriate if
  • 00:00:31
    the mixtures of
  • 00:00:32
    one or more drugs is mixed or there are
  • 00:00:35
    adult trends in the drug
  • 00:00:37
    still this test will work drug in
  • 00:00:40
    different forms
  • 00:00:41
    like gels transdermal patches the micro
  • 00:00:44
    questions
  • 00:00:45
    test will be useful in such kind of
  • 00:00:48
    complications also
  • 00:00:50
    some small scale forensic science
  • 00:00:52
    laboratories may lack
  • 00:00:53
    certain type of automated instruments
  • 00:00:56
    most of them
  • 00:00:57
    are having light microscopes and also
  • 00:01:00
    personals and scientists
  • 00:01:03
    but this instruments are not developed
  • 00:01:06
    if they are having proper experience
  • 00:01:07
    with microscopes
  • 00:01:09
    and they know how to observe the
  • 00:01:10
    crystals properly this is the most
  • 00:01:12
    efficient one
  • 00:01:14
    microcrystal tests use polarized light
  • 00:01:16
    microscopy
  • 00:01:18
    specially can identify most illicit
  • 00:01:20
    drugs
  • 00:01:21
    specifically and quickly usually within
  • 00:01:24
    few minutes
  • 00:01:25
    they are fast easy to perform and can be
  • 00:01:29
    highly specific and inexpensive compared
  • 00:01:32
    to other methods
  • 00:01:33
    in addition proper use of light
  • 00:01:35
    microscopy
  • 00:01:36
    and crystal tests can check and confirm
  • 00:01:40
    the results obtained by alternative
  • 00:01:42
    methods
  • 00:01:43
    i have provided a link in the
  • 00:01:45
    description where it ha
  • 00:01:47
    describes about polarized light
  • 00:01:49
    microscopy that is of nikon
  • 00:01:52
    and it is worth watching applied for
  • 00:01:54
    crystals
  • 00:01:55
    and its observation so
  • 00:01:59
    micro crystal test techniques are based
  • 00:02:02
    on highly developed
  • 00:02:03
    chemical precipitation reactions in
  • 00:02:05
    which a polarized microscope is used to
  • 00:02:08
    observe
  • 00:02:08
    distinguish the different types of
  • 00:02:10
    crystals formed
  • 00:02:11
    microcrystal tests are conformatory
  • 00:02:13
    tests often used to verify the results
  • 00:02:16
    of pulmonary screening methods
  • 00:02:18
    in history microcrystalline tests are
  • 00:02:21
    used to confirmation of sample
  • 00:02:23
    identification after doing a color test
  • 00:02:26
    and now it is still considered as a
  • 00:02:28
    confirmation test
  • 00:02:29
    but it is a wet lab method currently
  • 00:02:33
    instrumental method analysis are
  • 00:02:35
    considered as more specific
  • 00:02:36
    and for accurate positive results
  • 00:02:40
    though we have microcrystalline tests we
  • 00:02:42
    have to use instrumental methods
  • 00:02:44
    to give positive confirmation of
  • 00:02:46
    identification which could be much
  • 00:02:48
    appropriate to submit a computerized
  • 00:02:50
    report than a manual report which is
  • 00:02:51
    produced by our
  • 00:02:52
    microcustomers microcrystal analytical
  • 00:02:55
    process
  • 00:02:56
    is a different procedure of chemistry
  • 00:02:58
    compared with any other types
  • 00:02:59
    like color test we can see this
  • 00:03:02
    particular subject needs expertise and
  • 00:03:04
    skills to interpret the complicated
  • 00:03:06
    results
  • 00:03:07
    as such of crystals
  • 00:03:12
    coming to advantages of microcrystalline
  • 00:03:14
    techniques
  • 00:03:15
    as i already said this method is
  • 00:03:17
    inexpensive
  • 00:03:18
    we will need only pure reagent
  • 00:03:20
    microscopes and
  • 00:03:22
    some basic lab apparatus it can be
  • 00:03:24
    referred as an
  • 00:03:25
    alternative to gcms and fdi and these
  • 00:03:27
    are very sophisticated instruments for
  • 00:03:29
    analysis
  • 00:03:31
    micro crystal tests are also environment
  • 00:03:33
    friendly
  • 00:03:34
    where there is no much hazardous part
  • 00:03:36
    involved
  • 00:03:37
    until and unless the apparatus are
  • 00:03:38
    mishandled test procedure also consumes
  • 00:03:41
    very less amount of reagent than
  • 00:03:43
    reagents which we
  • 00:03:44
    consume to conduct instrumental analysis
  • 00:03:47
    there is no requirement of purification
  • 00:03:49
    for the compounds for analysis
  • 00:03:51
    this method is highly specific and
  • 00:03:52
    crystals are uniquely formed
  • 00:03:54
    only to specific reagents it should be
  • 00:03:57
    noted that microcrystalline formation
  • 00:03:59
    does not affect the chemical and
  • 00:04:00
    physical properties of substance this is
  • 00:04:03
    an
  • 00:04:03
    advantage so that you can use this
  • 00:04:05
    particular
  • 00:04:06
    sample which is been done for micro
  • 00:04:09
    crystal where you are adding the reagent
  • 00:04:11
    and you can do the instrumental analysis
  • 00:04:13
    further
  • 00:04:15
    one of the important advantage is that
  • 00:04:18
    the compounds with different
  • 00:04:19
    optical isomerism exhibit similar kind
  • 00:04:22
    of chemical and physical properties
  • 00:04:24
    and at that time differentiation would
  • 00:04:26
    not be possible
  • 00:04:27
    unless we when we are using polarimeter
  • 00:04:31
    so in this case test different
  • 00:04:34
    optical isomerisms exhibit different
  • 00:04:37
    crystal formations
  • 00:04:38
    hence we can differentiate the compounds
  • 00:04:40
    easily
  • 00:04:42
    sometimes the isomer may be a drug but
  • 00:04:44
    its complementary isomer may not be a
  • 00:04:46
    drug
  • 00:04:47
    so identification of isomer is also
  • 00:04:49
    crucial
  • 00:04:50
    which can attain by this
  • 00:04:54
    coming to disadvantage of micro
  • 00:04:56
    crystalline techniques
  • 00:04:58
    the principal disadvantage of micro
  • 00:05:00
    crystalline testing is that it is not
  • 00:05:01
    applicable to all substances
  • 00:05:03
    crystal testing procedures do not exist
  • 00:05:05
    for a number of commonly encountered
  • 00:05:07
    controlled substances and chemicals
  • 00:05:10
    microcrystal
  • 00:05:11
    testing can produce more than one type
  • 00:05:13
    of arrangement
  • 00:05:14
    presence of additional crystal forming
  • 00:05:16
    agents may interfere
  • 00:05:18
    the precipitation of target compound
  • 00:05:21
    this interference may cause either
  • 00:05:23
    distortions
  • 00:05:24
    or variations in the expected crystal
  • 00:05:27
    form
  • 00:05:27
    that is also known as polymorphism
  • 00:05:30
    this may complicate the identification
  • 00:05:32
    process in such cases a purification
  • 00:05:35
    procedure
  • 00:05:36
    is need to be done by thin layer
  • 00:05:38
    chromatography or any extraction method
  • 00:05:41
    this is recommended before micro
  • 00:05:43
    crystalline analysis has been done
  • 00:05:45
    the formation of solid crystalline
  • 00:05:48
    solution begins
  • 00:05:49
    when individual molecule or ions
  • 00:05:51
    clustered together
  • 00:05:53
    this process of nucleation continues
  • 00:05:55
    until a visible particle appears
  • 00:05:57
    in a crystal formation if the
  • 00:06:01
    sample material is having high
  • 00:06:03
    concentration then there is a fast
  • 00:06:04
    formation of crystal
  • 00:06:06
    which will engulf the debris in the
  • 00:06:08
    subject and there will be distortion in
  • 00:06:10
    the crystal observation
  • 00:06:12
    it will be not visible very clearly if
  • 00:06:14
    it is having many debris or if it is
  • 00:06:16
    having
  • 00:06:16
    high concentration therefore it is
  • 00:06:19
    required to pre-process the sample
  • 00:06:21
    if it is concentrated in the nature
  • 00:06:25
    so it is need to be pre-processed even
  • 00:06:28
    though
  • 00:06:28
    there is a point in advantages saying
  • 00:06:30
    that no purification is required
  • 00:06:34
    though there are standards available to
  • 00:06:36
    conf to compare
  • 00:06:37
    and identify this crystals formed this
  • 00:06:40
    process and interpret
  • 00:06:42
    interpretation of outcomes completely
  • 00:06:44
    depend upon the expertise of personal
  • 00:06:46
    doing the
  • 00:06:47
    test they should be having proper
  • 00:06:50
    capabilities to differentiate polymorph
  • 00:06:52
    crystal and identify individual
  • 00:06:54
    compounds from a mixture
  • 00:06:56
    if the sample is contaminated
  • 00:06:58
    microcrystalline tests lack versatility
  • 00:07:01
    due to which it is not suitable for
  • 00:07:03
    quantization and
  • 00:07:04
    documentation it is a special test which
  • 00:07:07
    needs
  • 00:07:07
    much attention and proper standards
  • 00:07:14
    micro crystal test techniques this is
  • 00:07:16
    the procedure
  • 00:07:18
    test sample is added with sufficient
  • 00:07:21
    amount of reagent
  • 00:07:22
    and there are some factors which should
  • 00:07:26
    be
  • 00:07:26
    considered while doing this test like
  • 00:07:29
    sometimes we need to
  • 00:07:31
    apply high temperature that means after
  • 00:07:33
    putting the
  • 00:07:34
    the sample and the reagent on the slide
  • 00:07:36
    we have to heat the slide
  • 00:07:38
    or sometimes it need to be kept in the
  • 00:07:40
    refrigerator to cool the temperature
  • 00:07:42
    or sometimes there is a requirement of
  • 00:07:44
    acid or bases
  • 00:07:46
    in the reagent so that ph is maintained
  • 00:07:48
    so these are the factors
  • 00:07:50
    uh part of preprocessing when
  • 00:07:53
    the sample is reacting with the reagent
  • 00:07:56
    there is formation of
  • 00:07:58
    solid why solid will be formed
  • 00:08:01
    molecules or ions cluster together
  • 00:08:04
    nucleation continues until a visible
  • 00:08:07
    particle appears
  • 00:08:08
    in a crystal formation this crystal
  • 00:08:10
    formation is unique
  • 00:08:12
    by its unique nature only we will be
  • 00:08:15
    able to identify
  • 00:08:16
    the sample okay this can be understood
  • 00:08:20
    in
  • 00:08:20
    three broad categories that is first one
  • 00:08:23
    aqueous techniques
  • 00:08:24
    aqueous technique is very simple take
  • 00:08:26
    the sample on the slide
  • 00:08:28
    take the rear joint on the slide but
  • 00:08:29
    separately two different tops are taken
  • 00:08:32
    separately like this
  • 00:08:34
    the sample reagent and the reagent
  • 00:08:37
    sample and the reagent separately are
  • 00:08:39
    taken and kept under the microscope
  • 00:08:41
    this two will be mixed under the
  • 00:08:43
    microscope itself
  • 00:08:44
    and you will be observing the formation
  • 00:08:46
    of crystals under the microscope
  • 00:08:48
    immediately while reaction is occurring
  • 00:08:51
    there is no requirement of coverslip for
  • 00:08:53
    this
  • 00:08:54
    so if you are doing late what will
  • 00:08:57
    happen
  • 00:08:57
    the saw crystals will form and the
  • 00:09:00
    complete sample will
  • 00:09:01
    solidify and you will be unable to
  • 00:09:03
    identify what type of
  • 00:09:04
    crystal it is next one volatility
  • 00:09:08
    technique in volatility technique we are
  • 00:09:10
    going to use
  • 00:09:11
    the slide which is having depression to
  • 00:09:14
    it
  • 00:09:15
    that means hanging drop slide
  • 00:09:19
    so in this depression we are going to
  • 00:09:21
    introduce the sample
  • 00:09:22
    and the sample nature here is volatile
  • 00:09:26
    so the volatile sample is going to
  • 00:09:28
    release vapors
  • 00:09:30
    so that is what our principle
  • 00:09:33
    is here take a cover slip on that
  • 00:09:36
    coverslip you place the reagent
  • 00:09:39
    and put the reagent over this depression
  • 00:09:42
    so there will be
  • 00:09:42
    some air gap between the actual sample
  • 00:09:45
    and our reagent they are not going to
  • 00:09:46
    get mixed
  • 00:09:48
    so in that air gap the vapors which are
  • 00:09:50
    released by the sample
  • 00:09:51
    are going to react with the reagent
  • 00:09:54
    when it is going to react with the
  • 00:09:56
    reagent there are crystal forms
  • 00:09:58
    formations which are seen on the
  • 00:10:00
    coverslip that can be observed from a
  • 00:10:02
    microscope so these crystals can be
  • 00:10:05
    unique and you can identify them
  • 00:10:08
    there is one more type of test that is
  • 00:10:11
    acid anionic test technique
  • 00:10:14
    this is the combination of aqueous and
  • 00:10:17
    volatility technique
  • 00:10:18
    a sample is placed in the cavity or the
  • 00:10:21
    depression
  • 00:10:22
    of a slide a drop of alcohol solution
  • 00:10:25
    methanol or ethanol is added one drop of
  • 00:10:28
    reagent is added
  • 00:10:30
    immediately after the alcohol and cover
  • 00:10:32
    slide is
  • 00:10:33
    placed over the cavity to prevent
  • 00:10:35
    evaporation
  • 00:10:36
    crystal formation is observed by placing
  • 00:10:38
    the cavity slide
  • 00:10:40
    with cover directly under a microscope
  • 00:10:43
    this technique is often used to
  • 00:10:45
    crystallize steroid hormones
  • 00:10:46
    barbiturates
  • 00:10:48
    including phenobarbital coming to
  • 00:10:50
    volatility technique
  • 00:10:51
    this is applied for observation of
  • 00:10:54
    volatile compounds like
  • 00:10:55
    aldehydes and ketones and also secondary
  • 00:10:58
    amines
  • 00:11:03
    so these are the few examples of micro
  • 00:11:05
    crystals which are formed and
  • 00:11:07
    the photographs are taken from the
  • 00:11:08
    microscope
  • 00:11:10
    so as like i already said microscope
  • 00:11:13
    which is use this
  • 00:11:14
    pluralized microscope and sometimes we
  • 00:11:16
    can also use
  • 00:11:17
    dark field microscope normal white light
  • 00:11:19
    microscope also to absorb this
  • 00:11:21
    crystals for more clarity for realized
  • 00:11:24
    micro microscope pieces
  • 00:11:26
    then these images are taken from a
  • 00:11:29
    macron
  • 00:11:30
    research institute they have given a
  • 00:11:31
    very good report
  • 00:11:33
    where all illicit drugs are tested micro
  • 00:11:35
    crystalline tests
  • 00:11:36
    and they have given different types of
  • 00:11:38
    crystals so this
  • 00:11:40
    particular report is used as reference
  • 00:11:43
    by many scientists who are doing the
  • 00:11:44
    narcotic drug analysis
  • 00:11:46
    or psychotropic drug analysis so let us
  • 00:11:49
    go into this mdma it is going to form
  • 00:11:53
    x type of crystals this these are one
  • 00:11:56
    kind of
  • 00:11:57
    crystals which are formed
  • 00:12:00
    by reacting with gold chloride so second
  • 00:12:03
    one method on
  • 00:12:05
    this is formed into rosette crystals
  • 00:12:06
    these are rosette crystals
  • 00:12:08
    which are able to see here by reacting
  • 00:12:10
    with mercuric chloride
  • 00:12:12
    these are cloth spins you can see this
  • 00:12:15
    shape is different from this this one
  • 00:12:18
    and
  • 00:12:18
    this is a d methamphetamine as like i
  • 00:12:21
    already said
  • 00:12:22
    optical isomers can also be identified
  • 00:12:25
    so this crystals are formed only to
  • 00:12:27
    d methamphetamine not for l type
  • 00:12:31
    okay next we are having morphine
  • 00:12:33
    morphine is going to form
  • 00:12:35
    a droplet kind of crystals these
  • 00:12:38
    crystals are little clumsy and
  • 00:12:40
    it is formed by glo gold bromide you can
  • 00:12:43
    see
  • 00:12:43
    all the four reagents which are used
  • 00:12:45
    here are a metal
  • 00:12:47
    with highlight combination and here also
  • 00:12:50
    we are having the same thing
  • 00:12:51
    oxycodone it is also forming a certain
  • 00:12:54
    kind of
  • 00:12:54
    crystals which can be said as rosettes
  • 00:12:58
    or it can also be uh tuft or bur
  • 00:13:01
    so this type of crystals are formed by
  • 00:13:04
    oxycodone
  • 00:13:06
    then pseudoephedrine a natural drug
  • 00:13:10
    it is been formed into tablets so these
  • 00:13:13
    particular structures can be referred as
  • 00:13:15
    tablets or plates so
  • 00:13:19
    this crystals are formed by deleteric
  • 00:13:21
    acid reacting with
  • 00:13:23
    pseudoephedrine and this one is cylosine
  • 00:13:26
    trinitrobenzoic acid is the reagent used
  • 00:13:29
    fan crystals so we can see fan crystals
  • 00:13:31
    here
  • 00:13:32
    these are very unique all drugs which i
  • 00:13:34
    have seen
  • 00:13:35
    among all cylosine is very unique
  • 00:13:38
    crystal which is formed
  • 00:13:40
    so that is a psychotropic drug coming to
  • 00:13:43
    cocaine
  • 00:13:44
    using a gold chloride gold chloride is
  • 00:13:47
    already seen in d methamphetamine
  • 00:13:48
    same reagent is again used for cocaine
  • 00:13:51
    in
  • 00:13:52
    methamphetamine we are going to see
  • 00:13:53
    cloth spins but in a cocaine we are
  • 00:13:55
    going to see
  • 00:13:56
    x-shaped crystals but this crystals are
  • 00:13:59
    very unique very
  • 00:14:00
    good design will be there if you see
  • 00:14:02
    this particular image
  • 00:14:03
    i am going to give you the link in the
  • 00:14:05
    description you just click on the link
  • 00:14:07
    you will be going into the
  • 00:14:08
    pdf file that is the report of this
  • 00:14:11
    micro crystalline test so that you will
  • 00:14:12
    be understanding all micro crystalline
  • 00:14:14
    tests
  • 00:14:15
    then diazepam a chemical of
  • 00:14:19
    benzodiazepines family and this is a
  • 00:14:22
    using
  • 00:14:22
    ammonium theocyanide so it is just like
  • 00:14:25
    a glass fracture that kind of uh with a
  • 00:14:28
    micro crystal is there but it is called
  • 00:14:30
    as rosette type
  • 00:14:32
    rosette type is here and again uh heroin
  • 00:14:35
    you can see mercury chloride
  • 00:14:37
    so mercury chloride it is repeated for
  • 00:14:39
    the second time
  • 00:14:40
    so we have already used it for methadone
  • 00:14:43
    it is forming rosettes
  • 00:14:44
    and for heroin it is forming feathery
  • 00:14:47
    dendrites
  • 00:14:48
    so if you are seeing this too it is
  • 00:14:51
    little uh
  • 00:14:53
    confused it is also almost similar but
  • 00:14:56
    you need to identify carefully
  • 00:14:57
    it is having feathery feathery kind of
  • 00:15:00
    crystals are formed
  • 00:15:01
    but here it is rosette type process type
  • 00:15:03
    means you can see
  • 00:15:05
    very particularly all are spreaded like
  • 00:15:08
    a star but here it is feathery type so
  • 00:15:11
    these are the types of crystals
  • 00:15:13
    and a very important tracks which are
  • 00:15:15
    been identified by using
  • 00:15:16
    the generally
  • 00:15:20
    combination of metals and highlights
  • 00:15:22
    that is commonly which we have seen
  • 00:15:26
    [Music]
  • 00:15:43
    [Music]
  • 00:16:00
    [Music]
  • 00:16:23
    thank you for watching friends i hope
  • 00:16:25
    this video was useful for you micro
  • 00:16:27
    crystalline tests are very important
  • 00:16:29
    and in very first slide itself i have
  • 00:16:31
    said you that
  • 00:16:32
    it is almost equivalent to instrumental
  • 00:16:34
    analysis but
  • 00:16:36
    micro crystalline tests are limited
  • 00:16:38
    because very few procedures are
  • 00:16:39
    available for very few chemicals
  • 00:16:41
    but instrumental methods of analysis we
  • 00:16:44
    can do any type of material
  • 00:16:46
    for examination and it will be very
  • 00:16:48
    helpful and the computerized
  • 00:16:49
    reports will be produced by that
タグ
  • Micro crystalline test
  • Drug identification
  • Forensic science
  • Polarized light microscopy
  • Crystal formation
  • Advantages
  • Disadvantages
  • Testing techniques
  • Optical isomers
  • Reagents